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1.
JAMA Dermatol ; 160(5): 544-549, 2024 May 01.
Artículo en Inglés | MEDLINE | ID: mdl-38506824

RESUMEN

Importance: Kindler epidermolysis bullosa is a genetic skin-blistering disease associated with recessive inherited pathogenic variants in FERMT1, which encodes kindlin-1. Severe orofacial manifestations of Kindler epidermolysis bullosa, including early oral squamous cell carcinoma, have been reported. Objective: To determine whether hypoplastic pitted amelogenesis imperfecta is a feature of Kindler epidermolysis bullosa. Design, Settings, and Participants: This longitudinal, 2-center cohort study was performed from 2003 to 2023 at the Epidermolysis Bullosa Centre, University of Freiburg, Germany, and the Special Care Dentistry Clinic, University of Chile in association with DEBRA Chile. Participants included a convenience sampling of all patients with a diagnosis of Kindler epidermolysis bullosa. Main Outcomes and Measures: The primary outcomes were the presence of hypoplastic pitted amelogenesis imperfecta, intraoral wounds, gingivitis and periodontal disease, gingival hyperplasia, vestibular obliteration, cheilitis, angular cheilitis, chronic lip wounds, microstomia, and oral squamous cell carcinoma. Results: The cohort consisted of 36 patients (15 female [42%] and 21 male [58%]; mean age at first examination, 23 years [range, 2 weeks to 70 years]) with Kindler epidermolysis bullosa. The follow-up ranged from 1 to 24 years. The enamel structure was assessed in 11 patients, all of whom presented with enamel structure abnormalities. The severity of hypoplastic pitted amelogenesis imperfecta varied from generalized to localized pitting. Additional orofacial features observed include gingivitis and periodontal disease, which was present in 90% (27 of 30 patients) of those assessed, followed by intraoral lesions (16 of 22 patients [73%]), angular cheilitis (24 of 33 patients [73%]), cheilitis (22 of 34 patients [65%]), gingival overgrowth (17 of 26 patients [65%]), microstomia (14 of 25 patients [56%]), and vestibular obliteration (8 of 16 patients [50%]). Other features included chronic lip ulcers (2 patients) and oral squamous cell carcinoma with lethal outcome (2 patients). Conclusions and Relevance: These findings suggest that hypoplastic pitted amelogenesis imperfecta is a feature of Kindler epidermolysis bullosa and underscore the extent and severity of oral manifestations in Kindler epidermolysis bullosa and the need for early and sustained dental care.


Asunto(s)
Epidermólisis Ampollosa , Humanos , Masculino , Femenino , Adulto , Adulto Joven , Preescolar , Adolescente , Niño , Epidermólisis Ampollosa/complicaciones , Persona de Mediana Edad , Estudios Longitudinales , Enfermedades Periodontales/complicaciones , Enfermedades Periodontales/epidemiología , Carcinoma de Células Escamosas/patología , Amelogénesis Imperfecta/complicaciones , Amelogénesis Imperfecta/genética , Amelogénesis Imperfecta/patología , Estudios de Cohortes , Neoplasias de la Boca/patología , Neoplasias de la Boca/complicaciones , Gingivitis/patología , Gingivitis/etiología , Queilitis , Chile
2.
Pediatr Transplant ; 15(8): 861-9, 2011 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-22112002

RESUMEN

We report the results of a prospective, standardized follow-up programme of eight children (median age at SCT 1.2 yr) with mucopolysaccharidosis (MPS1H, M. Hurler) transplanted using a fludarabine-based SCT. SCT resulted in stable engraftment without transplant-related mortality. All patients are alive, engrafted and in ambulatory care. During follow-up (median five yr, 1.9-8 yr), six of eight showed developmental delay (two severe, two mild/no), all eight had spinal deformities and one received hip surgery for acetabular dysplasia. Hand surgery for carpal tunnel release and trigger digits was required in five of the patients. The cranio-cervical junction was narrowed in four patients, one child having already received surgery. CC was present in all patients prior to SCT. It remained unchanged in seven and regressed in one child. Severe cardiac dysfunction was present in two of the eight children before SCT. Cardiac pump function was normal in six patients and ameliorated in two, while valve abnormalities could be detected in six patients. Currently, transplantation seems no longer the major obstacle for MPS1H patients, but the variable musculoskeletal disease progression after successful SCT remains a challenge. Patients with Hurler syndrome need specialized follow-up care because of their manifold health problems. The standardized follow-up presented here is a step to optimize care for MPS children and their families after SCT.


Asunto(s)
Progresión de la Enfermedad , Mucopolisacaridosis I/terapia , Trasplante de Células Madre , Preescolar , Femenino , Estudios de Seguimiento , Humanos , Lactante , Masculino , Mucopolisacaridosis I/fisiopatología , Trasplante Homólogo
3.
Am J Infect Control ; 48(6): 708-712, 2020 06.
Artículo en Inglés | MEDLINE | ID: mdl-32234262

RESUMEN

Alcohol-based hand disinfection is the key measure to prevent healthcare-associated infections and nosocomial transmission of pathogens. We conducted a survey among dental students, trainee nurses and medical technical assistants in training from the Generation Z to determine their knowledge regarding hand hygiene and to optimize education. Overall knowledge was worthy of improvement. Females performed better than males. Specifically tailored efforts seem necessary to increase hand hygiene competence in the Generation Z.


Asunto(s)
Infección Hospitalaria , Higiene de las Manos , Enfermeras y Enfermeros , Estudiantes de Medicina , Infección Hospitalaria/prevención & control , Femenino , Adhesión a Directriz , Desinfección de las Manos , Conocimientos, Actitudes y Práctica en Salud , Humanos , Masculino , Estudiantes de Odontología , Encuestas y Cuestionarios
4.
Spec Care Dentist ; 40 Suppl 1: 3-81, 2020 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-33202040

RESUMEN

BACKGROUND: Inherited epidermolysis bullosa (EB) is a genetic disorder characterized by skin fragility and unique oral features. AIMS: To provide (a) a complete review of the oral manifestations in those living with each type of inherited EB, (b) the current best practices for managing oral health care of people living with EB, (c) the current best practices on dental implant-based oral rehabilitation for patients with recessive dystrophic EB (RDEB), and (d) the current best practice for managing local anesthesia, principles of sedation, and general anesthesia for children and adults with EB undergoing dental treatment. METHODS: Systematic literature search, panel discussion including clinical experts and patient representatives from different centers around the world, external review, and guideline piloting. RESULTS: This article has been divided into five chapters: (i) general information on EB for the oral health care professional, (ii) systematic literature review on the oral manifestations of EB, (iii) oral health care and dental treatment for children and adults living with EB-clinical practice guidelines, (iv) dental implants in patients with RDEB-clinical practice guidelines, and (v) sedation and anesthesia for adults and children with EB undergoing dental treatment-clinical practice guidelines. Each chapter provides recommendations on the management of the different clinical procedures within dental practice, highlighting the importance of patient-clinician partnership, impact on quality of life, and the importance of follow-up appointments. Guidance on the use on nonadhesive wound care products and emollients to reduce friction during patient care is provided. CONCLUSIONS: Oral soft and hard tissue manifestations of inherited EB have unique patterns of involvement associated with each subtype of the condition. Understanding each subtype individually will help the professionals plan long-term treatment approaches.


Asunto(s)
Anestesia Dental , Epidermólisis Ampollosa Distrófica , Epidermólisis Ampollosa , Adulto , Niño , Humanos , Salud Bucal , Guías de Práctica Clínica como Asunto , Calidad de Vida
5.
Oper Dent ; 33(2): 155-62, 2008.
Artículo en Inglés | MEDLINE | ID: mdl-18435189

RESUMEN

This study evaluated the shear bond strength of self-etch adhesives to enamel and the effect of additional phosphoric acid etching. Seventy sound human molars were randomly divided into three test groups and one control group. The enamel surfaces of the control group (n=10) were treated with Syntac Classic (SC). Each test group was subdivided into two groups (each n=10). In half of each test group, ground enamel surfaces were coated with the self-etch adhesives AdheSe (ADH), Xeno III (XE) or Futurabond NR (FNR). In the remaining half of each test group, an additional phosphoric acid etching of the enamel surface was performed prior to applying the adhesives. The shear bond strength was measured with a universal testing machine at a crosshead speed of 1 mm/minute after storing the samples in distilled water at 37 degrees C for 24 hours. Fracture modes were determined by SEM examination. For statistical analysis, one-way ANOVA and the two-sided Dunnett Test were used (p>0.05). Additional phosphoric etching significantly increased the shear bond strength of all the examined self-etch adhesives (p<0.001). The highest shear bond strength was found for FNR after phosphoric acid etching. Without phosphoric acid etching, only FNR showed no significant differences compared to the control (SC). SEM evaluations showed mostly adhesive fractures. For all the self-etch adhesives, a slight increase in mixed fractures occurred after conditioning with phosphoric acid. An additional phosphoric acid etching of enamel should be considered when using self-etch adhesives. More clinical studies are needed to evaluate the long-term success of the examined adhesives.


Asunto(s)
Grabado Ácido Dental/métodos , Recubrimiento Dental Adhesivo , Esmalte Dental/ultraestructura , Recubrimientos Dentinarios/química , Ácidos Fosfóricos/química , Resinas Acrílicas/química , Adhesividad , Resinas Compuestas/química , Análisis del Estrés Dental/instrumentación , Humanos , Ensayo de Materiales , Metacrilatos/química , Microscopía Electrónica de Rastreo , Cementos de Resina/química , Resistencia al Corte , Estrés Mecánico , Propiedades de Superficie , Temperatura , Factores de Tiempo , Agua/química
6.
Blood ; 108(1): 362-9, 2006 Jul 01.
Artículo en Inglés | MEDLINE | ID: mdl-16537806

RESUMEN

We report on the molecular etiology of an unusual clinical phenotype associating congenital neutropenia, thrombocytopenia, developmental delay, and hypopigmentation. Using genetic linkage analysis and targeted gene sequencing, we defined a homozygous genomic deletion in AP3B1, the gene encoding the beta chain of the adaptor protein-3 (AP-3) complex. The mutation leads to in-frame skipping of exon 15 and thus perturbs proper assembly of the heterotetrameric AP-3 complex. Consequently, trafficking of transmembrane lysosomal proteins is aberrant, as shown for CD63. In basal keratinocytes, the incorporated immature melanosomes were rapidly degraded in large phagolysosomes. Despite distinct ultramorphologic changes suggestive of aberrant vesicular maturation, no functional aberrations were detected in neutrophil granulocytes. However, a comprehensive immunologic assessment revealed that natural killer (NK) and NKT-cell numbers were reduced in AP-3-deficient patients. Our findings extend the clinical and molecular phenotype of human AP-3 deficiency (also known as Hermansky-Pudlak syndrome, type 2) and provide further insights into the role of the AP-3 complex for the innate immune system.


Asunto(s)
Complejo 3 de Proteína Adaptadora/genética , Subunidades beta de Complejo de Proteína Adaptadora/genética , Eliminación de Gen , Síndrome de Hermanski-Pudlak/genética , Adolescente , Adulto , Análisis Mutacional de ADN/métodos , Síndrome de Hermanski-Pudlak/inmunología , Síndrome de Hermanski-Pudlak/patología , Homocigoto , Humanos , Células Asesinas Naturales/inmunología , Datos de Secuencia Molecular , Mutación , Neutrófilos/inmunología , Linaje , Fenotipo
7.
J Oral Maxillofac Surg ; 63(3): 304-10, 2005 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-15742278

RESUMEN

PURPOSE: The aim of the present study was to assess the influence of suture splinting for 1 week or rigid fixation for 4 weeks on final root length, root length increment, and mobility of autotransplanted immature third molars. PATIENTS AND METHODS: The sample consisted of 63 patients with a total of 65 transplanted immature third molars. All transplants had reached one-half (n = 29) to three-fourths (n = 36) of their expected root length. In 24 of the transplants, postoperative fixation was carried out with a rigid acid-etch composite and wire splint for 4 weeks (rigid group), and in 41 transplants, with a suture splint for 1 week (suture group). The fixation method depended on the initial stability of the transplants. All transplants were followed up clinically and radiologically for a mean period of 3.9 years. RESULTS: Transplants in the rigid group revealed a significantly lower final root length ( P = .002) and root length increment ( P = .001) than those in the suture group. The differences were found to be more pronounced in transplants at earlier developmental stages. No differences were found in transplant mobility. CONCLUSIONS: The results of the present study indicate that prolonged rigid fixation of autotransplanted immature third molars has a significantly negative influence on final root length and root length increment, especially in transplants at earlier developmental stages.


Asunto(s)
Tercer Molar/trasplante , Odontogénesis/fisiología , Férulas (Fijadores) , Técnicas de Sutura , Raíz del Diente/crecimiento & desarrollo , Adolescente , Adulto , Resinas Compuestas , Diseño de Equipo , Femenino , Estudios de Seguimiento , Humanos , Masculino , Tercer Molar/diagnóstico por imagen , Tercer Molar/fisiología , Odontometría , Radiografía , Acero Inoxidable , Corona del Diente/anatomía & histología , Movilidad Dentaria/etiología , Raíz del Diente/anatomía & histología , Raíz del Diente/diagnóstico por imagen , Alveolo Dental/cirugía , Trasplante Autólogo
8.
Dent Traumatol ; 18(6): 322-8, 2002 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-12656866

RESUMEN

Different data were published documenting the influence of fixation methods and periods on the outcome of autotransplantations of teeth. Besides studies reporting increased ankylosis and disturbances of pulpal revascularization following rigid or extended fixation, there are studies revealing no connection in this matter. The clinical and radiological results of 76 transplanted germs of third molars were to be assessed after a rigid fixation for 4 weeks or after a suture splinting for 7 days and compared with each other. The choice of fixation method depended on the initial stability of the transplant. After a mean observation period of 3.4 years (range 1.0-6.1 years), 92.9% of the teeth stabilized with a suture, but only 73.5% fixed with an acid-etch composite and wire splint could be classified as successful (P = 0.029). The significant increases in ankylosis (P = 0.036) and pulp necrosis (P = 0.041) were the factors for the less favorable results of the rigidly fixed teeth. Our data support the results of other experimental and clinical studies with regard to the negative influences of an extended and rigid fixation on the success of tooth transplantation. However, apart from a correlation with the method and period of fixation, we also suspect the influence of an incongruity between the transplant and recipient site.


Asunto(s)
Tercer Molar/trasplante , Ferulas Periodontales , Germen Dentario/trasplante , Adolescente , Adulto , Recubrimiento Dental Adhesivo , Pulpa Dental/irrigación sanguínea , Necrosis de la Pulpa Dental/etiología , Sensibilidad de la Dentina/etiología , Femenino , Humanos , Masculino , Resorción Radicular/etiología , Suturas , Anquilosis del Diente/etiología , Trasplante Autólogo/efectos adversos
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