Impact of Molar Incisor Hypomineralization on Oral Health-Related Quality of Life in Brazilian Schoolchildren Aged 8 to 10 Years

ABSTRACT Objective: To assess the impact of Molar Incisor Hypomineralization (MIH) and confounding factors on oral health-related quality of life (OHRQoL) according to the perception of 8 to 10-year-old children and their parents/caregivers. Material and Methods: A cross-sectional study including 403 students aged 8-10 years was carried out, in which OHRQoL was measured using the Child Perceptions Questionnaire administered to both children and parents/caregivers. The diagnosis of MIH was performed according to the previously proposed index. Dental caries experience, malocclusion, and sociodemographic factors were evaluated as confounders. Cluster analysis and Poisson regression with robust variance (p<0.05) were performed. Results: The prevalence of MIH was 13.4%. Parents/caregivers of children with MIH in incisors showed a higher impact prevalence in the emotional well-being domain (PR=1.92; 95%CI=1.16-3.19). Children with hypoplasia had a higher prevalence of negative impact on OHRQoL in the oral symptoms domain (PR=1.51; 95%CI=1.03-2.23). According to the perception of parents/caregivers, dental caries experience had a negative impact on the quality of life of students in the emotional well-being domain (PR=4.19; 95%CI=1.06-16.49) and in the total questionnaire score (PR=3.21; 95%CI=1.06-9.71). Conclusion: According to the perception of parents/caregivers, children with MIH in incisors showed a greater impact on OHRQoL. Additionally, the presence of hypoplasia affected the self-perception of OHRQoL in children, and caries experience influenced the OHRQoL of children, as perceived by parents/caregivers.

Knowledge of Dentists about Hypomineralization Enamel Defects: A Cross-Sectional Study

ABSTRACT Objective: To evaluate a group of Brazilian dentists on their knowledge of Molar Incisor Hypomineralization (MIH) and Hypomineralized Second Primary Molars (HSPM) related to clinical aspects, consequences, and diagnostic criteria. Material and Methods: In this cross-sectional, the participants were invited by e-mail and Whatsapp® to answer a questionnaire about their knowledge of hypomineralization enamel defects (MIH/HSPM) on the Google Forms® platform. The questionnaire comprised eight questions about personal data and multiple-choice questions about their knowledge concerning clinical aspects, diagnostic criteria of MIH/HSPM and differential diagnosis through clinical images. Chi-square test was applied with the significance level set at 5%. Results: Most participants (n = 492; 91.1%) reported having knowledge about MIH/HSPM. The general dentists gave more incorrect answers (n = 40; 65.6 %;) about dental tissues affected by MIH/HSPM. Overall, 83.3% of the dentists gave the correct answer to which dentitions are associated with this condition. In addition, most dentists presented knowledge about the consequences related to possible fractures (n= 487; 90.2%) and about an increased risk of caries (n= 479; 88.9%) in the affected teeth. Regarding the differential diagnosis performed through clinical images, most participants gave incorrect answers (p≤0.001). Conclusion: The participants presented knowledge about the dentition associated with this condition and possible consequences related to the teeth affected by MIH/HSPM; however, they showed difficulties concerning clinical diagnostic criteria.

Prevalence of Dental Fear and its Association with Painful Oral Conditions in Adolescents

ABSTRACT Objective: To estimate the prevalence of dental fear and evaluate its association with dental caries and with Molar Incisor Hypomineralization (MIH) in schoolchildren aged 11-14 years. Material and Methods: A cross-sectional study was conducted with 375 adolescents in Campina Grande, Brazil. Socioeconomic and oral health information was collected, while dental fear was measured using the Children's Fear Survey Schedule-Dental Subscale (CFSS-DS). The diagnosis of dental caries and MIH was performed by three trained examiners (κ ≥ 0.61) using the International Caries Detection & Assessment System - ICDAS II and a previously validated index, respectively. Data were descriptively analyzed using the Chi-Square, Fisher's Exact, and Poisson regression tests with robust variance (p<0.05). Results: The prevalence of dental fear was 18.4%, and the mean CFSS-DS total score was 28.96 ± 8.92. After adjusting for covariates family structure, schooling of parents/guardians, type of dental health service and dental pain in the last six months, the prevalence of dental fear was associated with dental pain in the last six months (PR=2.03; 95%CI=1.31-3.16; p=0.002). Conclusion: Although no association was found between dental fear, dental caries and MIH in adolescents, those who experienced dental pain in the last six months had a higher prevalence of dental fear.

Rehabilitation Treatment in Pediatric Patients with Molar Incisor Hypomineralization: A Scoping Review

ABSTRACT Objective: To identify the available evidence on the different treatment types for the rehabilitation of MIH-affected teeth in children. Material and Methods: A search was carried out in Pubmed, Cochrane Library, Epistemonikos, Lilacs and Google Scholar. Observational studies published until June 2022 were included. Two reviewers independently screened studies and extracted data. Results: 1593 studies were screened and a total of 38 articles were included, which were mainly case reports published in Brazil. Most included studies concluded that the evaluated treatment was "beneficial" or "probably beneficial". Reported treatments included: glass ionomer cements (GIC), composite resin restorations, preformed metal crowns, laboratory fabricated crowns, microabrasion management of incisors and resin infiltration. Conclusion: Successful treatment options have been identified, such as GIC as a provisional restoration for severe cases and for uncooperative children; restorations with composite, indirect restorations, or preformed metal crowns also seem suitable treatment options for young patients diagnosed with MIH. There is still little evidence to support an approach for anterior teeth affected by MIH.

Manifestaciones orales en paciente infantil con síndrome de Ellis-van Creveld: informe de caso / Manifestações orais em paciente infantil com síndrome de Ellis-van Creveld: relato de caso / Oral manifestations in child patient with Ellis-van Creveld syndrome: case report

El síndrome de Ellis-van Creveld es un trastorno autosómico recesivo caracterizado por una tétrada de enanismo desproporcionado, displasia ectodérmica, polidactilia postaxial y malformaciones cardíacas congénitas. En este artículo, presentamos el caso de un niño brasileño de 6 años con síndrome de Ellis-van Creveld que presentó un número notable de características orales y dentales clásicas y hallazgos poco comunes como taurodontismo. El examen clínico reveló hipoplasia múltiple del esmalte, surco vestibular ausente, aserraduras alveolares en la región anterior del maxilar, dientes ausentes, dientes cónicos, canino inferior girado, mordida cruzada posterior bilateral, caries dental y un nódulo. Radiográficamente se observa agenesia dentaria, taurodontismo de molares primarios y permanentes y retraso en la erupción dentaria. Los hallazgos clínicos y radiográficos pueden estar presentes desde el nacimiento y el odontopediatra tiene un papel fundamental en el diagnóstico precoz del síndrome de Ellis-van Creveld, así como en la prevención de problemas orales, rehabilitación e intervenciones estéticas.

A síndrome de Ellis-van Creveld é uma doença autossômica recessiva caracterizada por uma tétrade de baixa estatura desproporcional, displasia ectodérmica, polidactilia pós-axial e malformações cardíacas congênitas. Neste artigo, será relatado um caso de um menino brasileiro de 6 anos de idade com síndrome de Ellis-van Creveld que apresenta um número notável de características orais e dentárias clássicas e achados incomuns como taurodontismo. Ao exame clínico foi revelado hipoplasia múltipla do esmalte, sulco vestibular ausente, serrilhas alveolares na maxila anterior, dentes ausentes, dentes cônicos, canino inferior rotacionado, mordida cruzada posterior bilateral, cárie dentária e um nódulo. Radiograficamente, foi observado agenesia dentária, taurodontismo de molares decíduos e permanentes e atraso na erupção dentária. Os achados clínicos e radiográficos podem estar presentes desde o nascimento e o odontopediatra tem papel fundamental no diagnóstico precoce da síndrome de Ellis-van Creveld, bem como na prevenção de problemas bucais, reabilitação e intervenções estéticas.

Ellis­van Creveld syndrome is an autosomal recessive disorder characterized by a tetrad of disproportionate dwarfism, ectodermal dysplasia, postaxial polydactyly, and congenital heart malformations. In this article, we hereby present a case of a 6-year-old Brazilian boy with Ellis­van Creveld syndrome who presented with a remarkable number of classical oral and dental features and uncommon findings such as taurodontism. Clinical examination revealed multiple enamel hypoplasia, absent vestibular sulcus, alveolar serrations in the maxilla anterior region, missing teeth, conical teeth, lower canine rotation, bilateral posterior crossbite, dental caries, and a nodule. Radiographically were observed teeth agenesis, taurodontism of deciduous and permanent molars, and delayed tooth eruption. Clinical and radiographic findings may be present from birth and the pediatric dentist has a fundamental role in the early diagnosis of Ellis­van Creveld syndrome, as well as oral problems prevention, rehabilitation, and aesthetic interventions.

Use of Images and Clinical Experience to Calibrate Dental Surgeons for the Diagnosis of Molar Incisor Hypomineralization

ABSTRACT Objective: To evaluate an imaging protocol for use as a diagnostic and calibration tool for dentists before and after practical activity. Material and Methods: Thirty photos of children's teeth with or without changes in dental enamel were selected and evaluated by a group of experienced dentists previously calibrated to establish the diagnosis defined as the gold standard. After instructions, the images were shown to a group of postgraduate dentists for free identification of dental changes. Subsequently, a lecture on molar incisor hypomineralization (MIH) was carried out, and, at 14 days and all calibration was performed using the criteria previously. The retest was performed at 28 days. After experience in clinical activity in the following two weeks, the post-test was performed at 49 days. Data were analyzed using Cohen's kappa coefficient. Results: Theoretical learning on the subject showed low inter-examiner agreement when the diagnosis of defects was made from images obtained from intraoral photographs. After clinical practice, there was greater intra-examiner agreement. After theoretical training, dentists started to identify different types of enamel alteration, although with low agreement between them. Conclusion: Clinical experience in theoretical and imaging training favored the identification of defects. However, it is necessary to improve the protocol to establish a reliable and viable diagnostic method for calibration in MIH.

Prevalencia de los defectos de desarrollo del esmalte de la especialidad de odontologia infantil en la UJAT 2021-2022 / Prevalência de defeitos de desenvolvimento do esmalte da especialidade de odontologia infantil da UJAT 2021-2022 / Prevalence of enamel development defects of the specialty of children's dentistry at the UJAT 2021-2022

Objetivo: Conocer la prevalencia de los Defectos del desarrollo del esmalte en pacientes de la especialidad de odontología infantil en la UJAT. Material y Método: Se realizó un estudio observacional, transversal, prospectivo, cuantitativo, que permitirá conocer la frecuencia y prevalencia de los defectos del esmalte en pacientes infantiles de la especialidad de odontología infantil de la UJAT. La población de estudio fue finita a conveniencia del investigador ya que se conoce el número de pacientes que integran el estudio. La investigación se llevó a cabo con un universo de 300 pacientes con una población analizada de entre 0 a 15 años de la cual se obtuvo una muestra de 195 pacientes durante el periodo 2021-2022, con un intervalo de confianza del 95% y un margen de error del 5%. Variables: edad, género, arcada con mayor afectación, cantidad de órganos dentales y tipo de dentición. Resultados: El defecto del esmalte más prevalente resultó ser Hipoplasia seguido del HIM, con afectación principalmente del sexo femenino y en la edad de 4 a 8 años, se observó que ambas arcadas son afectadas, que la dentición mixta es la más afectada, los órganos dentales más afectados fueron los incisivos centrales y los 1ros molares, en relación con los antecedentes perinatales no se presentó alguna complicación como mayor afectación. Conclusiones: El principal defecto de la estructura del esmalte es la Hipoplasia y la presentan más las mujeres y el rango de edad donde se observó la mayor prevalencia es de 4 a 8 años

Objetivo: Conhecer a prevalência de defeitos de desenvolvimento do esmalte em pacientes especializados em odontologia infantil na UJAT. Material e Método: Foi realizado um estudo observacional, transversal, prospectivo, quantitativo, que permitirá conhecer a frequência e prevalência de defeitos de esmalte em pacientes crianças da especialidade de odontologia infantil da UJAT. A população do estudo foi finita para a conveniência do investigador, uma vez que o número de pacientes no estudo é conhecido. A pesquisa foi realizada com um universo de 300 pacientes com população analisada entre 0 e 15 anos de idade, dos quais foi obtida uma amostra de 195 pacientes no período de 2021 a 2022, com intervalo de confiança de 95% e margem de erro de 5%. Variávis: idade, sexo, arco com maior envolvimiento, número de órgaõs dentários e tipo de dentição. Resultados: O defeito do esmalte mais prevalente foi a Hipoplasia seguida pela HIC, com acometimento principalmente feminino e na idade de 4 a 8 anos, observou-se que ambos os arcos são acometidos, que a dentição mista é a mais acometida, os órgãos dentários mais afetados foram os incisivos centrais e os 1º molares, Em relação à história perinatal, não houve complicação como maior envolvimento. Conclusões: O principal defeito da estrutura do esmalte é a hipoplasia e é mais apresentado pelas mulheres e a faixa etária onde a maior prevalência foi observada é de 4 a 8 anos

Objective: To determine the prevalence of enamel defects in patients of the Specialty in Pediatric Dentistry in the UJAT. Material and Method: An observational, cross-sectional, prospective, quantitative study was carried out, which allowed to know the frequency and prevalence of enamel defects in child patients of the Specialty in Pediatric Dentistry at the UJAT. The study population was finite at the convenience of the researcher since the number of patients that make up the study is know. The research was carried out with a universe of 300 patients with a population analyzed population between 0 and 15 years of age from which a sample of 195 patients was obtained during the period 2021-2022, with a confidence interval of 95% and a margin of error of 5%. Variables: age, gender, arch with greater involvement, number of dental organs and type of dentition. Results: The most prevalent enamel defect turned out to be Hypoplasia followed by MIH, affecting mainly females and between the ages of 4 and 8 years, it was observed that both arches are affected, that the mixed dentition is the most affected, the most affected teeth stated were the central incisors and the first molars; In most cases, the perinatal history stated there was no complication as greater involvement. Conclusions: The main defect if enamel structure is Hypoplasia and it is presented more bye the women and the age range where the highest prevalence was observed is from 4 to 8 years

Manifestações bucais em portadores de epidermólise bolhosa residentes em um município baiano / Oral manifestations of epidermolysis bullosa in a municipality of the state of Bahia

Introdução: a Epidermólise Bolhosa hereditária (EB) é uma doença rara, caracterizada por formações de bolhas na pele e nas mucosas que sofrem mínimos traumas ou aparecem espontaneamente. As principais divisões de EB são Epidermólise Bolhosa Simples, Epidermólise Bolhosa Juncional, Epidermólise Bolhosa Distrófica e a Síndrome de Kindler. As manifestações bucais geralmente encontradas nos pacientes com EB são as bolhas no epitélio oral, microstomia, anquiloglossia, doença periondontal, hipoplasia do esmalte, cárie dentária, atrofia da maxila e prognatismo mandibular, variando para cada tipo da doença. Objetivo: relatar as manifestações bucais dos portadores de Epidermólise Bolhosa residentes no município de Barra da Estiva. Metodologia: trata-se de um estudo transversal, quantitativo e descritivo que foi desenvolvido no município de Barra da Estiva ­ BA com a população de portadores de Epidermólise Bolhosa, através da realização de anamnese e exame clínico. Estatística descritiva foi utilizada para tabular os dados coletados. Resultados: foram analisados 5 portadores de Epidermólise Bolhosa, a maioria do sexo masculino (60%), com média de idade de 5,6 anos. As manifestações bucais encontradas foram bolhas orais (100%), anquiloglossia (100%), língua despapilada (100%), hipoplasia de esmalte (80%), cárie (40%) e abertura de boca limitada em média de 28,6 mm. Conclusão: os portadores de Epidermólise Bolhosa apresentaram manifestações orais características da doença, tendo como consequências maiores dificuldades para realizar higienização bucal e tratamento odontológico, sendo necessário conhecimento prévio dos cirurgiões-dentistas para o atendimento desses pacientes.

Introduction: inherited Epidermolysis Bullosa (EB) is a rare disease, characterized by blistering of the skin and mucous membranes that suffer minimal trauma or appear spontaneously. The main divisions of EB are Simple Epidermolysis Bullosa, Junctional Epidermolysis Bullosa, Dystrophic Epidermolysis Bullosa and Kindler Syndrome. The oral manifestations usually found in patients with EB are blisters in the oral epithelium, microstomy, ankyloglossia, periodontal disease, enamel hypoplasia, dental caries, atrophy of the jaw and mandibular prognathism, varying for each type of disease. Objective: to report the oral manifestations of Epidermolysis Bullosa patients living in the municipality of Barra da Estiva. Methods: cross-sectional study, quantitative and descriptive that was developed in the municipality of Barra da Estiva-BA with the population of people with Epidermolysis Bullosa, through anamnesis and clinical examination. Descriptive statistics was used to tabulate the data collected. Results: 5 children with Epidermolysis Bullosa were analyzed, most male (60%), with an average age of 5,6 years. Oral manifestations found were oral blisters (100%), anquiloglossia (100%), loss of papillae of the tongue (100%), enamel hypoplasia (80%), tooth decay (40%) and mouth opening limited to the average of 28.6 mm. Conclusion: epidermolysis Bullosa children presented oral manifestations common to the disease, leading to difficulties in performing oral hygiene and dental treatment, requiring prior knowledge of dental surgeons for the care of these patients.

Enfoque de Tratamiento de una Adolescente con Amelogénesis Imperfecta / Treatment Approach for an Adolescent with Amelogenesis Imperfecta

La amelogénesis imperfecta (AI) es un grupo de tras-tornos hereditarios, clínica y etiológicamente hete-rogéneos, derivados de mutaciones genéticas, que se caracterizan por anomalías cualitativas y cuanti-tativas del desarrollo del esmalte, pudiendo afectar la dentición primaria y/o permanente. El tratamiento del paciente con AI es complejo y multidiscliplinario; supone un desafío para el odontólogo, ya que por lo general están involucradas todas las piezas dentarias y afecta no solo la salud buco dental sino el aspecto emocional y psicológico de los pacientes. Con el obje-tivo de describir el tratamiento integral y rehabilita-dor realizado en una paciente con diagnóstico de AI tipo III, se reporta el caso de un adolescente de sexo femenino de 13 años, que concurrió en demanda de atención a la Cátedra de Odontología Integral Niños de la Facultad de Odontología de la Universidad de Buenos Aires (FOUBA), cuyo motivo de consulta fue la apariencia estética y la hipersensibilidad de sus pie-zas dentarias. Durante el examen clínico intraoral, se observó que todas las piezas dentarias presentaban un esmalte rugoso, blando, con irregularidades y una coloración amarronada, compatible con diagnóstico de Amelogénesis Imperfecta tipo III hipomineralizada. Conclusión: El tratamiento rehabilitador de la AI en los pacientes en crecimiento y desarrollo estará diri-gido a intervenir de manera integral y temprana para resolver la apariencia estética y funcional, evitar las repercusiones sociales y emocionales, y acompañar a los pacientes y sus familias (AU)

Amelogenesis imperfecta (AI) is a group of clinically and etiologically heterogeneous hereditary disorders, derived from genetic mutations, characterized by qualitative and quantitative anomalies of enamel development, which can affect primary and/or permanent dentition. The treatment of patients with AI is complex and multidisciplinary, it is a challenge for the dentist, since in general all the teeth are involved and it affects not only oral health but also the emotional and psychological aspect of the patients. Objective: To describe the comprehensive and rehabilitative treatment carried out in an adolescent patient with a diagnosis of type III AI. Case report: The case of a 13-year-old female patient, who required dental attention at the Department of Dentistry for Children of the School of Dentistry of the University of Buenos Aires, whose reason for consultation was esthetic appearance and hypersensitivity of her teeth. In the intraoral clinical examination, it was observed that all the teeth had rough, soft enamel, with irregularities and a brownish color, compatible with the diagnosis of type III hypomineralized Amelogenesis Imperfecta. Conclusion: Rehabilitative treatment of AI in growing and developing patients will be aimed at early and comprehensive intervention to resolve esthetic and functional appearance, avoid social and emotional repercussions and accompany patients and their families (AU)

Systemic Manifestations, Tooth Eruption and Enamel Defects in Children with Congenital Zika Virus Syndrome: 36-Month Follow-up Case Series

Abstract Objective: To describe systemic manifestations, the characteristics related to tooth eruption, and the occurrence of enamel defects in children with Congenital Zika Virus Syndrome (CZS). Material and Methods: Prospective case series based on nine children with confirmed CZS diagnosis assisted at a reference center in a municipality in the Northeast Region of Brazil. Through a structured interview directed to mothers, information related to prenatal, delivery, and postpartum periods was collected. Tooth eruption was monitored through clinical examinations for 36 months. The modified developmental defect of enamel index (DDE) was used to identify opacities and hypoplasia. Data were presented using descriptive statistics. Results: A high proportion (77.8%) had microcephaly, and 55.5% had low birth weight. Musculoskeletal disorders, swallowing difficulty, and self-injury practices were present in all children. Among the systemic findings, visual impairment (77.8%) and seizures (77.8%) were widely reported. Concerning disorders related to the stomatognathic system, bruxism (66.7%) and difficulty in sucking (33.3%) were present. For most children (77.8%), the deciduous right lower central incisor was the first tooth to erupt (minimum 8 months and maximum 17 months). Enamel defects were diagnosed in only two children (22.2%). Conclusion: A wide range of systemic manifestations was observed in children with CZS, including visual impairment and musculoskeletal disorders. Delayed eruption of the first deciduous tooth was also observed. Enamel defects were present in a small proportion of children.

El impacto de la hipomineralización molar incisivo en la calidad de vida de los niños brasileños / O impacto da hipomineralização molar incisivo na qualidade de vida de crianças brasileiras / The impact of molar incisor hypomineralization in the quality of life in Brazilian school children

El objetivo de este estudio fue verificar la prevalencia de HMI, la severidad y el impacto en la calidad de vida de niños de 8 a 10 años. Un total de 864 niños de ambos sexos fueron evaluados en la ciudad de Vila Velha, ES. La valoración clínica del HMI estuvo de acuerdo con los criterios diagnósticos de la EAPD. Como criterio de exclusión de la investigación se consideraron niños con déficit cognitivo, neuropsicomotor y pacientes con aparatología de ortodoncia. La condición leve o severa se determinó evaluando la necesidad de tratamiento 1 y la afectación de los incisivos y molares permanentes. Para evaluar el impacto en la calidad de vida se aplicó el Cuestionario de Percepción Infantil, con 29 preguntas relacionadas con síntomas orales, limitaciones funcionales, bienestar emocional y social. Los resultados se analizaron después de las pruebas estadísticas: Chi Cuadrado, Fischer y Poisson. Se encontró una frecuencia de 183 niños (21 %) con HMI, 125 (68,3 %) con el tipo severo que necesita tratamiento. En la aplicación de CPQ, la sensibilidad y el dolor en los dientes afectados tuvieron una puntuación más alta, y cuando asociado con la presencia o ausencia del HMI, los individuos afectados tuvieron un mayor impacto en este dominio (P = 0,04). Se concluye que el HMI afecta la población estudiada en condición severa, requiriendo cuidados odontológicos preventivos y reparadores, y puede tener un impacto negativo en la calidad de vida de los estudiantes en relación a su salud bucal, en cuanto a síntomas bucales.

O objetivo deste estudo foi verificar a prevalência da HMI, a severidade e o impacto na qualidade de vida, em crianças dos 8 aos 10 anos de idade. Foi avaliado um total de 864 crianças de ambos os sexos, na cidade de Vila Velha, ES. A avaliação clínica da HMI foi de acordo com os critérios diagnósticos da EAPD. Como critério de exclusão da investigação foram consideradas crianças com déficits cognitivos, neuropsicomotores e portadoras de aparelhos ortodônticos. A condição leve ou severa foi determinada através da avaliação da necessidade de tratamento 1 e do envolvimento de molares e incisivos permanentes. Para avaliar o impacto na qualidade de vida, foi aplicado o Questionário de Percepção Infantil, composto por 29 perguntas relacionadas aos sintomas orais, limitações funcionais, bem-estar emocional e social. Os resultados foram analisados após os testes estatísticos: Chi Square, Fischer e Poisson. Foi encontrada uma frequência de 183 crianças (21 %) com HMI, com 125 (68,3 %) com o tipo severo a necessitar de tratamento. Na aplicação do CPQ, a sensibilidade e a dor nos dentes afetados apresentaram uma pontuação mais elevada, e quando este instrumento foi associado à presença ou ausência do HMI, os indivíduos afetados também tiveram um maior impacto neste domínio (P = 0,04). Concluímos que a HMI afeta a população estudada na condição do tipo severa, exigindo cuidados dentários preventivos e restauradores, e pode ter um impacto negativo na qualidade de vida dos estudantes em relação à sua saúde oral, no que diz respeito aos sintomas orais.

Purpose of this study was to verify the prevalence of MIH, the severity and the impact on the quality of life, in children from 8 to 10 years of age. Materials and methods: A total of 864 children of both genders, in the city of Vila Velha, ES, were evaluated. The clinical assessment followed the diagnostic criteria of the EAPD. As exclusion criterion of the research were children with cognitive deficits, neuropsychomotor and carriers orthodontic appliances. The mild or severe conditions were determined by assessing the need for treatment (WHO) and involvement of permanent molars and incisors. To evaluate the impact on quality of life, the Child Perception Questionnaire was applied, composed of 29 questions elaborated to observe the child's perception regarding oral symptoms, functional limitations, well-being Emotional and social. For statistical analysis, Chi, Square, Fischer and Poisson tests were used. Results: A frequency of 183 children (21%) with MIH was found, with 125 (68.3%) with the severe type requiring treatment. In the application of CPQ, the sensitivity and pain in affected teeth presented a higher score, and when this instrument was associated with the presence or absence of MHI, the affected individuals also had a greater impact in this domain (P = 0.04). Conclusions: The MIH affects the studied population in severe condition, requiring preventive and restorative dental care, and can negatively impact the quality of life of the students in relation to their oral health, as far as oral symptoms are concerned

Prevalence and predisponent factors of molar-incisor hypomineralization in primary dentition

Aim: To evaluate the prevalence and predisposing factors for hypomineralization of second molars in children in primary dentition. Methods: A questionnaire was applied to parents to analyze predisposing factors and to assist in the diagnosis of hypomineralization in children between 2 and 6 years old, followed by an intraoral examination based on indices of non-fluorotic enamel defects in the primary dentition, according to the "Modified Index DDE" to determine demarcated opacity and HSPM presence / severity index to assess hypomineralization. Children from public and private schools were dived into two groups: if they presented HSPM-Group 1 (G1) and if they did not have HSPM-Control group (CG). Results: The most frequent predisposing factors associated with the child were Illness in the first year of life (X2= 6.49; p=0.01) and antibiotic use in the first year of life (X2= 41.82; p= 0.01). The factors associated with the mother were hypertension (X2= 9.36; p=0.01), infections during pregnancy (X2=14.80; p=0.01) and alcohol consumption during pregnancy (X2=97.33; p=0.01). There was a prevalence of 3.9% of HSPM in 14 children, with statistical difference regarding gender (X2 = 4.57; p <0.05), with boys presenting a higher frequency. In G1 hypomineralization was of the type with demarcated opacity, with more prevalent characteristics the yellowish spot, with moderate post-eruptive fracture and acceptable atypical restorations. All lesions were located in the labial region with 1/3 of extension. Conclusion: The prevalence of HSPM in children between 2 and 6 years old was 3.9%, with a predominance in males, with tooth 65 being the most affected. There was an association between HSPM and infection in the first year of life, as well as the use of antibiotics and sensitivity in the teeth affected by the lesion. There was an association between HSPM and hypertension, infection and mothers' alcohol use during pregnancy

Técnica minimamente invasiva em lesão branca hipoplásica: relato de caso / Minimally invasive technique in hypoplastic white injury: case report / Técnica minimamente invasiva en lesiónblancahipoplástica: caso clínico

Introdução:As manchas dentárias, dentre elas a hipoplasia do esmalte,corresponde a um dos motivos que fazem com que os pacientes busquem alterações no seu sorriso.O tratamento proposto deve ser sempre o mais conservador possível e buscar devolver a autoestima do paciente. Objetivo:Este trabalho objetivou apresentarum relato de caso clínico de paciente do sexo feminino, 26 anos, insatisfeita com a estética do seu sorriso por apresentar dentes escurecidos e hipoplasia de esmalte na face vestibular, em incisivo superior.Descrição do caso:Ao exame clínico foi observado escurecimento fisiológico e hipoplasia de esmalte no incisivo lateral superior esquerdo (22).O plano de tratamento proposto foi clareamento dental pela técnica associada (técnica de consultório + técnica caseira), remoção da mancha hipoplásica de formaminimamente invasiva e restauração em resina composta direta. Conclusões:Através de um correto diagnóstico, associado a uma técnica e seleção de material adequado, foi possível conseguir excelência estética com preservação de estrutura dentária sadia (AU).

Introduction:Dental stains, including enamel hypoplasia, correspond to one of the reasons that make patients seek changes in their smile. The proposed treatment should always be as conservative as possible and seek to restore the patient's self-esteem.Objective:This study aimedto present a clinical case report of a 26-year-old female patient, dissatisfied with the aesthetics of her smile as she had darkened teeth and enamel hypoplasia on the vestibular face, in anupper incisor. Case description:On clinical examination, physiological darkening and enamel hypoplasia were observedon the left upper lateral incisor (22). The proposed treatment plan was dental bleaching using the associated technique (In-office bleaching+ at-home bleaching), removal of the hypoplastic stain in a minimally invasive manner and restoration in direct composite resin.Conclusions:Through a correct diagnosis, associated with a technique and selection of suitable material, waspossible to achieve aesthetic excellence with preservation of healthy dental structure (AU).

ntroducción: Las manchas dentales, incluida la hipoplasia del esmalte, corresponden a una de lasrazones que hacenquelos pacientes busquencambios em susonrisa. El tratamiento propuestosiempredebe ser lo másconservador posible y tratar de restablecerla autoestima del paciente.Objetivo: Este estudio tuvo como objetivo presentarun informe de caso clínico de una paciente de 26 años de edad, insatisfechacon la estética de susonrisa, ya que habíaoscurecidolosdientes y la hipoplasia del esmalte en lasuperficie vestibular, en el incisivo superior.Descripcióndel caso: Enelexamen clínico, se observó oscurecimiento fisiológico e hipoplasia del esmalte en el incisivo lateral superior izquierdo (22). El plan de tratamiento propuestofueel blanqueamiento dental utilizando la técnica asociada (técnica de consultorio + técnica casera), eliminación de la mancha hipoplásica de maneramínimamente invasiva y restauraciónen resina compuestadirecta. Conclusiones: A través de un diagnóstico correcto, asociado con una técnica y selección de material adecuado, fueposible lograr laexcelencia estética conlapreservación de una estructura dental sana (AU).

Clinical and Molecular Disorders Caused by COVID-19 During Pregnancy as a Potential Risk for Enamel Defects

ABSTRACT This paper discusses the potential risk that COVID-19 generates for the development of enamel defects. This hypothesis was built based on the etiopathogenesis of enamel defects and the relationship with the symptom's characteristic of COVID-19. Pregnancy is a critical period for the child's development; exposure to pathological agents can cause systemic imbalances and risks of adverse perinatal and prenatal outcomes. The main clinical symptoms of this disease and its association with that dental outcome were considered. Fever, breathing, cardiovascular disorders, and diarrhea were related as potential etiological factors of ameloblast metabolism imbalance, which can interfere qualitatively and quantitatively in the development, maturation and mineralization of the tooth enamel. Molecular disorders derived from COVID-19, as well as their clinical symptoms, can be considered potential risk factors for the development of enamel defects. Individuals with enamel defects experienced high stress levels during pregnancy or early childhood. The approach adopted may help build new research to ensure understanding of the etiology of the development of dental enamel defects and its relationship with COVID-19. However, longitudinal studies need to be conducted to confirm the association between COVID-19 and adverse events during pregnancy.

Presence of molar-incisor hypomineralization is associated with dental caries in Brazilian schoolchildren

Abstract This study aimed to identify the prevalence of molar-incisor hypomineralization (MIH) in schoolchildren and its association with dental caries experience. This was a cross-sectional study with a sample of 471 children aged 8 to 10 years. Data were collected via a sociodemographic questionnaire. Intra-oral clinical examination was done to identify and diagnose MIH (EAPD Criteria) as well as dental caries (ICDAS Index). Statistical analyses were performed with Person's Chi-square, Fisher's exact, and Mann-Whitney tests, and Poisson regression models were built. Statistical significance was set at an alpha-level of 0.05. The prevalence of MIH in our participants was 9.8%, with lesions being mostly of the mild form (65.2%) and affecting the first permanent molars but not the incisors in 54.2% of the children. Dental caries was observed in 88.1% of subjects. We observed a significant association between dental caries and the following variables: presence of MIH (p < 0.01; PR = 1.13), dental visit (p < 0.02; PR=0.92), and parents or legal guardians' education level (p < 0.05; PR = 1.07). A MIH diagnosis was also significantly associated with family income (p < 0.05; PR = 4.09). Children with MIH had more caries lesions on molar surfaces (p < 0.01; PR = 4.05). The prevalence of MIH was found to be moderate, based on previous studies, and the presence of enamel defect was associated with dental caries. The teeth most affected by MIH lesions were the first permanent molars.

Inheritance pattern of molar-incisor hypomineralization

Abstract The aim of this study was to investigate the segregation patterns of molar incisor hypomineralization (MIH) in families, given the evidence that its etiology is influenced by genetics. Clinically, MIH may be detected in parents and/or siblings of MIH-affected children. Our study included children with at least one first permanent molar affected by MIH (proband) and their first-degree relatives (parents and siblings). The participants were examined clinically to detect MIH, according to the European Academy of Paediatric Dentistry criteria (2003). A total of 101 nuclear families (391 individuals) were studied. Proband diagnosis was followed by MIH classification of the subject, his parents and siblings, as affected, unaffected, or unknown. Segregation analysis was performed using the multivariate logistic regression model of the Statistical Analysis for Genetic Epidemiology package, and segregation models (general transmission, environmental, major gene, dominant, codominant and recessive models). The Akaike information criterion (AIC) was used to evaluate the most parsimonious model. In all, 130 affected individuals, 165 unaffected individuals, and 96 unknown individuals were studied. Severe MIH was found in 50.7% of the cases. A segregation analysis performed for MIH revealed the following different models: environmental and dominance (p = 0.05), major gene (p = 0.04), codominant (p = 0.15) and recessive models (p = 0.03). According to the AIC values, the codominant model was the most parsimonious (AIC = 308.36). Our results suggest that the codominant model could be the most likely for inheriting MIH. This result strengthens the evidence that genetic factors, such as multifactorial complex defect, influence MIH.

What are the Systemic Factors Associated with the Molar-Incisor Hypomineralization Etiology?

ABSTRACT Objective: To evaluate the systemic factors associated with Molar-Incisor Hypomineralization (MIH) etiology. Material and Methods: A total of 731 8-year-old schoolchildren enrolled in the public school system in Curitiba, Brazil, was randomly selected. The MIH diagnosis was performed by calibrated examiners (Kappa >0.80) according to the European Academy of Pediatric Dentistry criteria (2003). The systemic factors were collected through a semi-structured questionnaire and applied to the children's mothers, addressing the medical history from pregnancy to the first three years of children's life. Associations were analyzed by Poisson regression analysis with robust variance (p<0.05). Results: The systemic factors in the prenatal and perinatal periods were not associated with MIH (p>0.05). The children who used medications during the first years of life had a significantly higher prevalence of MIH (PRc = 2.18 CI = 95% 1.06-4.48; p=0.033). Conclusion: The use of medications during the first three years of children's life is associated with a higher prevalence of MIH.

Dentists' Knowledge and Clinical Experience towards Molar-Incisor-Hypomineralization in Iran

ABSTRACT Objective: To determine the knowledge and clinical experience of dentists regarding MIH in Kerman/Iran. Material and Methods: In this cross-sectional study, a census sampling method was used, and all dentists registered in Kerman medical council were asked to participate in the study. A validated and reliable researcher administered questionnaire was used to determine participants' demographic characteristics, knowledge, and clinical experience. The association between knowledge score and demographic variables was determined using an independent t-test and ANOVA. The level of significance was set as 0.05. Results: Overall, 400 specialized and general dentists in Kerman completed the questionnaire. The mean knowledge score of dentists was 6.6±1.9 of 11. Female dentists' knowledge was higher than male dentists (p<0.05). General dentists had a higher level of knowledge regarding MIH compared to specialists (p<0.05). Overall, 79.5 % had been faced with MIH during their practice years. After confronting MIH teeth, 48.8% of dentists referred patients to specialists for treatment. Providing aesthetics was considered the most difficult part of treatment (43.2%). Resin composite was the most favorable dental material for treating MIH (60.9%). Conclusion: Although most dentists in Kerman had encountered MIH defects during their clinical practice, they did not have enough knowledge of the defect and required education on all aspects of MIH diagnosis and management. Younger dental practitioners, general dentists and females presented higher knowledge of MIH.

Diagnóstico y tratamiento de hipomineralización molar primaria en gemelos: reporte de un caso / Diagnóstico e tratamento de hipomineralização molar decíduo em gêmeos: Relato de caso / Diagnosis and treatment of deciduous molar hypomineralization in twins: Case report

Los defectos del esmalte dental en la dentición primaria en niños con antecedentes de prematuridad y bajo peso son frecuentes. Una de las causas de la prematuridad es el embarazo gemelar, que hace que la mayoría de los fetos sean prematuros debido al crecimiento intrauterino restringido. El objetivo de este trabajo es informar de la importancia de un diagnóstico correcto y precoz de la hipomineralización de los molares deciduos (HMD) en gemelos prematuros, así como de las posibilidades de tratamiento. Materiales y métodos: Dos niñas gemelas idénticas de 5 años que presentaban el mismo patrón de HMD en los dientes 55,65,75,85 ya con gran destrucción e historia de sensibilidad. Ya habían recibido atención odontológica, pero sólo una de las hermanas recibió tratamiento restaurador, la segunda no permitió el tratamiento, se utilizaron técnicas de manejo de la conducta, pero no fue posible realizar procedimientos operatorios. En el examen clínico y radiográfico se constató la posibilidad de realizar la técnica de Hall en los dientes 55,65 de la gemela 1 y 85 de la gemela 2. Resultados: Los dientes 75 y 85 de l a gemela 1, fueron diagnosticados clínica y radiográficamente con necesidad de restauración en resina compuesta, ya que estaban con restauraciones provisionales y asintomáticos. Los dientes 55 y 65 de lagemela 2 recibieron restauraciones ionoméricas y el diente 75 recibió una pulpectomía y una corona de acero. Conclusión: La técnica de Hall es muy bienvenida cuando se trata de rehabilitaciones en hipoplasia, especialmente cuando se trata del manejo de la edad joven, todavía hay diagnósticos erróneos cuando se examina una HMD(hipomineralización molar primaria)

Defeitos de esmalte dentário na dentição decídua são comuns em crianças com histórico de prematuridade e baixo peso. Uma das causas da prematuridade é a gestação gemelar, esta faz com que a maioria dos fetos sejam prematuros devido ao crescimento intrauterino restrito. O objetivo deste trabalho é relatar a importância de um diagnóstico correto e precoce de Hipomineraliação Molar Decíduo (HMD) em gêmeos prematuros, e as possibilidades de tratamento. Materiais e Métodos: duas crianças 5 anos sexo feminino gêmeas univitelinas que possuíam o mesmo padrão de HMD nos dentes 55,65,75,85 já com grande destruição e histórico de sensibilidade. As mesmas já receberam atendimento odontológico, porém apenas uma das irmãs recebeu tratamento restaurador, a segunda irmã não permitiu tratamento, técnicas de gestão comportamental foram utilizadas, mas não foi possível a realização dos procedimentos operatórios. Em exame clínico e radiográfico constatou-se a possibilidade de execução da técnica Hall nos dentes 55,65 da gêmea 1 e 85 da gêmea 2. Resultados: Os dentes 75 e 85 da gêmea 1, foram diagnosticados clinicamente e radiograficamente com necessidade restauradoraem resina composta,pois estavam com restaurações provisórias e assintomáticos. Os dentes 55 e 65 da gêmea 2 receberam restaurações ionoméricas e o dente 75 pulpectomia e coroa de aço. Conclusão: A Hall Technique é muito bem-vinda quando se trata de reabilitações em hipoplasias, principalmente no que tange ao manejo de pouca idade, ainda existem erros de diagnóstico na hora de examinar uma HMD (Hipomineralização Molar Decíduo)

Dental enamel defects in the primary dentition are common in children with a history of prematurity and low birth weight. One of the causes of prematurity is twin pregnancy, which causes most cases to be premature due to restricted intrauterine growth. The objective of this report is to relate the importance of a correct and early diagnosis and as treatment alternatives for of Deciduous Molar Hypomineraliation (DMH) in premature twins. Materials and methods: 5 years old, female, identical twins who had the same HMD pattern in their teeth 55,65,75,85 presented with a long history of destruction and sensitivity. They had previously received dental care. Only one of the sisters received restorative treatment. The other sister did not have

Evaluación orofacial de los niños Síndrome Prader-Willi / Avaliação orofacial de crianças com Síndrome de Prader-Willi / Orofacial assessment of children with Prader-Willi Syndrome

Resumen Objetivo: Evaluar el estado de salud bucal y el crecimiento craneofacial de pacientes con síndrome de Prader-Willi (SPW), en comparación con niños obesos que no padecen SPW. Métodos y resultados: Se seleccionaron 40 niños con SPW y 40 controles obesos de 10,9 años de edad (control: 11,89 años) y un IMC de 22,72 kg / m2 (control de 36,43 kg / m2). La evaluación de la salud oral ha incluído el número de dientes, tipo de dentición, presencia de caries, sangrado gingival, maloclusión, acumulación de placa, erosión dental, hiperplasia gingival e hipoplasia del esmalte. Los cuestionarios evaluaron los hábitos de higiene oral. Las radiografías panorámicas evaluaron el crecimiento craneofacial. El grupo de casos tenía un 6,8% menos de dientes en comparación con el grupo de control. Se observó una diferencia estadísticamente significativa en el sangrado gingival, la erosión dental y la hipoplasia del esmalte (p = 0,009; p = 0,02 y p = 0,006, respectivamente). Aunque no hubo diferencias estadísticamente significativas, se observó un número aumentado de lesiones cariosas y apiñamiento dental en niños con SPW (p = 0,35 y p = 0,07). Ambos grupos mostraron mala higiene dental. Los niños con SPW mostraron un crecimiento de la rama mandibular aumentada en comparación con el control (p = 0.03). Conclusión: Los niños con SPW tenían hemorragia gingival estática aumentada e hipoplasia del esmalte que los controles con obesidad no SPW. Los niños con SPW pueden presentar un crecimiento vertical craneofacial

Objetivo: Avaliar a saúde bucal e o crescimento craniofacial de pacientes pediátricos com SíndromedePrader-Willi(SPW),emcomparação a crianças obesas não-sindrômicas. Métodos e resultados: Foram selecionadas 40 crianças com SPW e 40 controles não obesos com SPW, com idade de 10,9 anos (controle: 11,89 anos) e IMC 22,72 kg / m2 (controle 36,43 kg / m2). Foram avaliados o número de dentes, tipo de dentição, presença de cárie, sangramento gengival, má oclusão, acúmulo de placa bacteriana, erosão dentária, hiperplasia gengival e hipoplasia do esmalte. Os questionários avaliaram os hábitos de higiene bucal. Radiografias panorâmicas avaliaram o crescimento craniofacial. O grupo caso teve um número 6,8% menor de dentes em comparação ao grupo controle. Observouse diferença estatisticamente significante no sangramento gengival, erosão dentária e hipoplasia do esmalte (p = 0,009; p = 0,02 e p = 0,006, respectivamente). Não houve diferença estatisticamente significante, observou-se um número aumentado de lesões de cárie e apinhamento dentário em crianças com SPW (p = 0,35 e p = 0,07). Ambos os grupos apresentaram má higiene dental. As crianças com SPW apresentaram crescimento aumentado do ramo mandibular com diferença estatisticamente significante (p = 0,03). Conclusão: As crianças com SPW apresentaram sangramento gengival estatisticamente aumentado e hipoplasia do esmalte do que os controles não obesos com SPW. Crianças com SPW podem apresentar crescimento vertical craniofacial aumentado. Mais investigações são necessárias para essa população.

Aim: To assess the oral health status and craniofacial growth of patients with Prader-Willi Syndrome (PWS), compared to obese non-PWS children controls. Methods and Result: 40 PWS children and 40 non-PWS obese controls, aged 10.9 years (control: 11.89 years) and BMI 22.72 kg/m2 (control 36.43 kg/m2) were selected. The number of teeth, type of dentition, presence of caries, gingival bleeding, malocclusion, plaque accumulation, dental erosion, gingival hyperplasia, and enamel hypoplasia were assessed. Questionnaires assessed oral hygiene habits. Panoramic radiographs assessed craniofacial growth. The study group had a 6.8% lower number of teeth compared to the control group. A statistically significant difference was seen in gingival bleeding, dental erosion and enamel hypoplasia (p=0,009; p=0,02 and p=0,006; respectively). There were no statistically significant differences, it was observed an augmented number of carious lesions and Although a higher prevalence of carious lesions and dental crowding was observed in PWS children, the difference was not satisctically significant (p=0.35 and p=0.07 respectively). Both groups showed poor dental hygiene. PWS children showed augmented mandibular ramus growth with a statistically significant difference (p=0.03). Conclusion: PWS children had statically augmented gingival bleeding and enamel hypoplasia than non-PWS obese controls. PWS children may present increased craniofacial vertical growth. Further investigations are needed for this population.