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1.
Eur Arch Paediatr Dent ; 21(1): 119-127, 2020 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-31190243

RESUMO

PURPOSE: Ectopic second premolars may lead to impaction and loss of space in the jaws, and in rare cases even to resorption of the first permanent molar. The aim of this study was to analyse different treatment strategies of ectopic second premolars and if possible give guidelines on when to favour different treatment approaches. MATERIALS AND METHODS: The study was a retrospective, non-randomised, outcome analysis of treatment on 41 ectopic second premolars in 37 patients (24 females and 13 males). In all cases oral examination, radiographs (pre-, peri-, and post) and full medical history were obtained. The treatment options included: (a) spontaneous eruption, (b) spontaneous eruption + extraction of primary tooth, (c) surgical exposure, (d) surgical uprighting, and (e) surgical uprighting + orthodontic extrusion. For evaluation each tooth was scored according to: (1) stage of root development, (2) distance between edges of the premolar and first permanent molar, (3) depth of impaction, (4) inclination, (5) horizontal position of the tooth. The level of significance was set to 5%. RESULTS: Only mild cases of ectopic second premolars are self-correcting. Based on the position of the tooth in the jaw different treatment options may be chosen, these may include: extraction of primary predecessor (impaction depth < 5 mm, inclination < 55°), surgical exposure of tooth germ (impaction depth < 5.5 mm, inclination < 95°) or surgical uprighting (impaction depth > 5.5 mm with no inclination limit). CONCLUSION: If there is no sign of self-correction after a short observation period, it is important to consider active treatment to help guiding the tooth into the correct eruption pathway.


Assuntos
Erupção Ectópica de Dente , Dente Impactado , Dente Pré-Molar , Feminino , Humanos , Masculino , Dente Molar , Estudos Retrospectivos , Erupção Dentária
2.
Eur Arch Paediatr Dent ; 20(3): 295-300, 2019 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-30904994

RESUMO

BACKGROUND: Primary failure of tooth eruption (PFE) is a rare non-syndromic disorder with prematurely ceased eruption of the posterior teeth, despite clearance by bone resorption of the eruption path. It is generally agreed that most of the impacted teeth are second molars that are deeply seated, and without symptoms. Traditionally, patients with failure of tooth eruption undergo surgical and/or orthodontic treatment. However, patients with PTH1R mutations have no beneficial effect of such a regime and PFE is therefore important to diagnose. CASE REPORT AND FOLLOW-UP: A family with three PFE affected members in two generations, involving both the primary and permanent dentitions, and a novel mutation in the PTH1R gene are reported. Furthermore, the treatment of the eruption failure was documented in one of the cases. CONCLUSION: In the present study, the proband initially only had a minor clinical problem, lack of eruption of the primary second left mandibular molar. However, over time several problems appeared in the permanent dentition. Clinical signs of PFE should lead one to look for similar dental problems in related family members and to molecular DNA testing. Confirmation of the diagnosis PFE in young children has the advantage that unnecessary treatment can be avoided, since early orthodontic intervention for these patients is futile. Once growth is complete, several multidisciplinary treatment strategies can partially solve the posterior open bite malocclusion that is characteristic of this disorder. Treatment should be planned in cooperation with specialists who are used to treating PFE patients.


Assuntos
Erupção Dentária , Dente Impactado , Criança , Pré-Escolar , Humanos , Dente Molar , Mutação , Receptor Tipo 1 de Hormônio Paratireóideo , Irmãos
3.
Orthod Craniofac Res ; 20(4): 196-201, 2017 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-28873288

RESUMO

OBJECTIVES: Studies have shown that the mandibular permanent first molar (M1inf ) in young children with isolated cleft palate is characterized by delay in maturation and has reduced crown width. Consequently, it is of interest to investigate the early maturation and width of the follicle and crown of M1inf in children with combined cleft lip and palate. DESIGN: Retrospective, longitudinal study. Cephalometric X-rays of 47 consecutive Danish children with UCCLP (37 males; 10 females) and 44 with unilateral incomplete cleft lip (UICL) (29 males; 15 females) examined at 2 and 22 months of age. UICL served as control group. Maturation (according to Haavikko), width of follicle (FW) and crown (CW) of M1inf were assessed. RESULTS: The maturation of the first mandibular molar was delayed in both genders at 2 and 22 months of age. FW and CW were smaller in children with UCCLP at both 2 and 22 months of age. There was a positive correlation between maturation and FW. CONCLUSIONS: Maturation of the first mandibular molar is delayed in both genders, and FW and CW were reduced in UCCLP compared to controls. Maturation was correlated with FW.


Assuntos
Fenda Labial/fisiopatologia , Fissura Palatina/fisiopatologia , Dente Molar/crescimento & desenvolvimento , Fatores Etários , Feminino , Humanos , Lactente , Estudos Longitudinais , Masculino , Mandíbula , Estudos Retrospectivos
4.
Cleft Palate Craniofac J ; 53(1): 3-15, 2016 01.
Artigo em Inglês | MEDLINE | ID: mdl-25844560

RESUMO

OBJECTIVE: Three-dimensional surface imaging is an increasingly popular modality for face measurements in infants with cleft lip and palate. Infants are noncompliant toward producing specific facial expressions, and selecting the appropriate moment of acquisition is challenging. The objective was to estimate amount and spatial distribution of deformation of the face due to facial expression in infants with cleft lip and palate and provide recommendations for an improved acquisition protocol, including a method of quality control in terms of obtaining images with true neutral expression. MATERIAL AND METHODS: Three-dimensional surface images of ten 4-month-old infants with unrepaired cleft lip and palate were obtained using a 3dMDface stereophotogrammetric system. For each subject, five surface images judged as representing a neutral expression were obtained during the same photo session. Mean and maximum deformations were calculated. A formalized review was performed, allowing the image exhibiting the "best" neutral expression to be selected, thus decreasing errors due to residual facial expression. RESULTS: Deformation due to facial expression generally increased from forehead to chin. The amount of deformation in three selected regions were determined: nose (mean, 1 mm; maximum = 3 mm); cleft region (mean, 2 mm; maximum = 5 mm); chin region (mean, 5 mm; maximum = 12 mm). Analysis indicated that introduction of a formalized review of images could reduce these errors by a factor of 2. CONCLUSIONS: The continuous change of facial expression in infants represents a substantial source of error; however, this may be reduced by incorporating a formalized review into the acquisition protocol.


Assuntos
Fenda Labial/patologia , Fissura Palatina/patologia , Expressão Facial , Imageamento Tridimensional/métodos , Fotogrametria/métodos , Pontos de Referência Anatômicos , Feminino , Humanos , Processamento de Imagem Assistida por Computador/métodos , Lactente , Masculino , Projetos Piloto
5.
Gesundheitswesen ; 77(7): 496-8, 2015 Jul.
Artigo em Alemão | MEDLINE | ID: mdl-26227383

RESUMO

A notification from a laboratory concerning the detection of Campylobacter jejuni in a 6-year-old boy initiated the investigation carried out by the health authorities from Stendal district, in order to explain the morbidity rate caused by the germ. The day after the boy's pediatrician informed about a visit to a farm, which was confirmed by the head of the nursery. She told the health authorities about the consumption of raw milk during their visit at the farm.The following days more children fell sick. Within 10 days the total number of diseased children was 21. The health authorities asked for stool samples of the diseased children, nursery nurses and the head of the farm since raw milk presents a potential cause of infection. The health authorities together with the Saxony-Anhalt State Office for Consumer Protection conducted a retrospective cohort study. The aim was to explain the association between the exposure from raw milk consumption and the occurrence of the disease from C. jejuni. Based on a questionnaire data about the food and milk intake at the nursery and at home and about the trip to the farm were collected. 91% of the children's cohort and 86% of the adults' cohort were captured.The exposed group at risk showed a higher risk of falling ill than the group, which was not exposed. The risk factor raw milk explained the difference. Furthermore, the analysis of milk samples taken by the district veterinary office from 2 cows and from the farm's tank was able to detect the germs. The correlation of the illness, the consumption of raw milk, the detection of C. jejuni in the samples taken from the children and the samples taken from the cows was evident. Based on the case the health authorities recommended that heads of nurseries as well as heads of dairy farming in the district of Stendal needed to be advised on raw milk. Nurseries are still allowed to take trips to farms. However, raw animal derivates including milk must not be consumed.


Assuntos
Infecções por Campylobacter/epidemiologia , Infecções por Campylobacter/microbiologia , Infecções por Campylobacter/prevenção & controle , Contaminação de Alimentos/estatística & dados numéricos , Doenças Transmitidas por Alimentos/epidemiologia , Leite/microbiologia , Animais , Campylobacter jejuni , Criança , Pré-Escolar , Surtos de Doenças , Contaminação de Alimentos/prevenção & controle , Microbiologia de Alimentos/estatística & dados numéricos , Doenças Transmitidas por Alimentos/microbiologia , Doenças Transmitidas por Alimentos/prevenção & controle , Alemanha , Humanos , Incidência , Berçários para Lactentes , Pasteurização , Saúde Pública , Estados Unidos
6.
Gesundheitswesen ; 77(7): 499-501, 2015 Jul.
Artigo em Alemão | MEDLINE | ID: mdl-26227384

RESUMO

Since 2012, there are not only trivalent inactivated influenza vaccines (TIV) but also live attenuated influenza vaccines (LAIV) available for children aged 2-17 years in Germany. The Saxony-Anhalt State Office for Consumer Protection conducted a test-negative case-control-study. The aim of the study was to identify the effectiveness of LAIV and TIV against a confirmed influenza diagnosis in children and adolescents in Saxony-Anhalt in the season 2012/13. The children had nasal swabs taken, which were further diagnosed in a laboratory using the PCR method. 834 patients of 15 voluntarily participating paediatric surgeries in Saxony-Anhalt were analysed by multivariate logistic regression with STATA 12. Controlling for age group, gender and month of the disease's onset showed an effectiveness of all vaccines amongst the 2-17 years old (38% with 95% CI: 0.8-61%; p=0.046). A differentiation according to LAIV and TIV demonstrated a significant effectiveness for LAIV (84%) in children of all ages (95% CI: 45-95%, p=0.004). After stratification for age groups LAIV was proven efficient in children aged 2-6 years (90% with 95% CI: 20-99%, p=0.03), whilst it led to a non-significant result in children aged 7-17 years (74% with 95% CI: -32-95%, p=0.106). There was no significant effectiveness of TIV seen in any age group.The Saxony-Anhalt State Office for Consumer Protection endorses the use of LAIV in children in accordance with the STIKO recommendations, as long as no contraindication is evident.


Assuntos
Vacinas contra Influenza/administração & dosagem , Influenza Humana/epidemiologia , Influenza Humana/terapia , Adolescente , Distribuição por Idade , Criança , Pré-Escolar , Feminino , Alemanha/epidemiologia , Humanos , Influenza Humana/diagnóstico , Masculino , Prevalência , Estudos Retrospectivos , Fatores de Risco , Distribuição por Sexo , Resultado do Tratamento , Vacinas Atenuadas/administração & dosagem , Vacinas de Produtos Inativados/administração & dosagem
7.
Prenat Diagn ; 35(6): 571-6, 2015 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-25663194

RESUMO

OBJECTIVES: The objective of this article is to investigate normal prenatal maxillary length using 3D ultrasound and to correlate this with previously reported results for the mandible and the biparietal diameter (BPD). METHODS: Seventy-two 3D ultrasound volumes from normal pregnancies in 52 volunteers (gestational age: 11-26 weeks) were obtained using a GE Voluson 730 Expert 3D scanner. Maxillary length and BPD were measured. Growth velocity and rate were calculated. Maxillary values were correlated with BPD and previously reported mandibular values. RESULTS: The mean total maxillary length ranged from 7.4 ± 2.7 mm at 11 weeks to 33.1 ± 2.7 mm at 26 weeks. Maxillary growth velocity can be described using a linear model. The correlation between maxillary and mandibular length, and BPD was high (R = 0.85-0.88). There was no statistically significant difference in the growth velocity between maxilla and mandible, whereas the velocity of the increase in BPD growth was significantly larger than that of the jaws. However, the growth rate was larger for the jaws than for the BPD. CONCLUSIONS: Normative measures for the maxilla in 11- to 26-week-old fetuses are presented. Change in maxillary length was described using a linear model. The maxillary and mandibular growth velocities and rates were similar but differ from those of the BPD.


Assuntos
Imageamento Tridimensional , Maxila/diagnóstico por imagem , Adulto , Cefalometria , Estudos Transversais , Feminino , Humanos , Maxila/embriologia , Tamanho do Órgão , Gravidez , Primeiro Trimestre da Gravidez , Segundo Trimestre da Gravidez , Estudos Prospectivos , Valores de Referência , Crânio/diagnóstico por imagem , Crânio/embriologia , Ultrassonografia Pré-Natal , Adulto Jovem
8.
Orthod Craniofac Res ; 17(2): 106-14, 2014 May.
Artigo em Inglês | MEDLINE | ID: mdl-24397533

RESUMO

OBJECTIVES: To estimate the influence of a short mandible on the risk of developing a cleft palate with/without a cleft lip (CP). SETTING AND SAMPLE POPULATION: The retrospective sample consisted of 115 2-month-old Danish infants with CP, and 70 control infants with unilateral incomplete cleft lip (UICL). MATERIAL AND METHODS: Cephalometric X-rays were obtained. Mandibular length (Lm ) was measured and corrected for body length (Lb ) to remove influence of varying body length in the sample. Logistic regression was applied to the corrected mandibular length (Lmc ) to calculate the risk of having a cleft palate. RESULTS: The mean mandibular length in the group with CP was about 4 mm shorter than in the control group. Odds ratio (OR) was calculated to be 0.58 (95% confidence interval 0.48-0.68), implying that an individual's risk of cleft palate with/without a cleft lip increases about 50% per mm decrease in mandibular length. CONCLUSIONS: A special facial type including a short mandible is a possible risk factor for cleft palate, and it was found that the risk of cleft palate increases 58% per mm decreases in mandibular length.


Assuntos
Fenda Labial/etiologia , Fissura Palatina/etiologia , Mandíbula/patologia , Pontos de Referência Anatômicos/diagnóstico por imagem , Pontos de Referência Anatômicos/patologia , Estatura , Peso Corporal , Cefalometria/métodos , Queixo/diagnóstico por imagem , Queixo/patologia , Humanos , Lactente , Funções Verossimilhança , Modelos Logísticos , Mandíbula/diagnóstico por imagem , Côndilo Mandibular/diagnóstico por imagem , Côndilo Mandibular/patologia , Radiografia , Retrognatismo/complicações , Estudos Retrospectivos , Fatores de Risco
9.
Fetal Diagn Ther ; 25(1): 36-9, 2009.
Artigo em Inglês | MEDLINE | ID: mdl-19169035

RESUMO

A 34-year-old Caucasian woman with cleidocranial dysplasia (CCD) and a known family history of CCD was referred for an ultrasound examination in the first trimester of her second pregnancy. Molecular genetic analysis of the RUNX2 gene was non-informative. A routine 2D ultrasound examination carried out at a local hospital at gestational age 12 weeks showed no signs of CCD. A 3D ultrasound examination in week 15+4 showed a fetus with typical CCD features including large fontanelles, lack of nasal bones, clavicles without the typical S-form, as well as severe delay in calvarial ossification, especially in the midline. Serial 3D ultrasound examinations during pregnancy confirmed the diagnosis, and over time the manifestations became even more distinct. The diagnosis was clinically confirmed at birth. This case suggests that the typical craniofacial CCD traits, including wide unmineralized areas in the calvarial midline and missing nasal bones, are easily recognizable using 3D ultrasound as early as in week 15.


Assuntos
Displasia Cleidocraniana/diagnóstico por imagem , Ultrassonografia Pré-Natal , Adulto , Displasia Cleidocraniana/genética , Feminino , Humanos , Gravidez
10.
Fetal Diagn Ther ; 24(2): 103-5, 2008.
Artigo em Inglês | MEDLINE | ID: mdl-18648208

RESUMO

OBJECTIVE: Early prenatal diagnosis of cleidocranial dysplasia (CCD) in a case in which molecular genetic analysis of the RUNX2 gene was non-informative. METHODS: 2D ultrasound examination. RESULTS: At week 13+6, a 2D ultrasound examination revealed a fetus with severely delayed ossification of the vertebral spine. The clavicles were barely seen and the calvarial bones were significantly less ossified than expected for gestational age. The fetus had otherwise normal anatomy and biometry. Serial ultrasound examinations during pregnancy confirmed the diagnosis, but the manifestations became less distinct. The diagnosis was confirmed clinically at birth. CONCLUSION: This case illustrates an early easily recognizable pattern of severely delayed ossification of the vertebral spine, which is probably a characteristic of CCD.


Assuntos
Displasia Cleidocraniana/diagnóstico por imagem , Osteogênese , Coluna Vertebral/diagnóstico por imagem , Ultrassonografia Pré-Natal , Adulto , Cesárea , Clavícula/diagnóstico por imagem , Displasia Cleidocraniana/embriologia , Displasia Cleidocraniana/genética , Subunidade alfa 1 de Fator de Ligação ao Core/genética , Feminino , Idade Gestacional , Humanos , Nascido Vivo , Linhagem , Gravidez , Crânio/diagnóstico por imagem , Coluna Vertebral/embriologia
11.
Cleft Palate Craniofac J ; 43(2): 160-7, 2006 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-16526921

RESUMO

OBJECTIVE: Analysis of early postnatal mandibular size and growth velocity in children with untreated isolated cleft palate (ICP), nonsyndromic Robin sequence (RS), and a control group of children with unilateral incomplete cleft lip (UICL). MATERIAL: 114 children (66 isolated cleft palate, 7 Robin sequence, 41 unilateral incomplete cleft lip) drawn from a group representing all Danish cleft children born from 1976 through 1981. All children were examined at both 2 and 22 months of age. METHODS: Cephalometric x-rays and maxillary plaster casts. Mandibular length and height were measured and mandibular growth velocity (mm/year) was calculated. Cleft width was measured on the casts at 2 months of age. RESULTS: Mean mandibular length and posterior height were significantly smaller in isolated cleft palate and Robin sequence, compared with unilateral incomplete cleft lip. Mandibular length in Robin sequence was also significantly shorter, compared with isolated cleft palate. No significant difference was found between mean mandibular growth velocities in the three groups. No significant correlation was found between mandibular length and cleft width in either isolated cleft palate or Robin sequence at 2 months of age. CONCLUSION: The children with isolated cleft palate and Robin sequence had small mandibles shortly after birth, but with a relatively normal growth potential. No true mandibular catch-up growth was found up to 22 months of age in either group. No significant correlation was found between mandibular size and cleft width in either group at 2 months of age. However, there was a significant trend toward the shorter the mandible, the more severe the sagittal extension of the cleft.


Assuntos
Fenda Labial/fisiopatologia , Fissura Palatina/fisiopatologia , Mandíbula/crescimento & desenvolvimento , Síndrome de Pierre Robin/fisiopatologia , Distribuição por Idade , Estudos de Casos e Controles , Cefalometria , Pré-Escolar , Fenda Labial/patologia , Fissura Palatina/patologia , Dinamarca , Feminino , Humanos , Lactente , Estudos Longitudinais , Masculino , Mandíbula/patologia , Palato/patologia , Síndrome de Pierre Robin/patologia , Distribuição por Sexo , Estatísticas não Paramétricas
12.
Diabet Med ; 22(11): 1566-73, 2005 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-16241923

RESUMO

AIMS: To study how structure and process of care is associated with outcome assessed by HbA(1c). METHODS: Data for this cross-sectional study originated from the nationwide Danish Registry for Childhood Diabetes and two questionnaires. One questionnaire was sent to all children under 16 years of age with Type 1 diabetes in the year 2000 (N = 1087, response rate 80%). Another questionnaire was sent to the 19 centres in Denmark treating these children (response rate 100%). Simultaneously the children were asked to take a blood sample for central HbA(1c) analysis. Linear mixed models were used for analysis of associations between structure and process indicators and HbA(1c). Age, diabetes duration, sex, ethnicity, family structure and parents' occupational status were included as patient factors possibly affecting HbA(1c). RESULTS: More visits to the outpatient clinic and higher insulin dosage were significantly associated with higher HbA(1c) (P = 0.002 and P = 0.0001, respectively). Increased frequency of blood glucose monitoring (BGM/week) and completed nephropathy screening were significantly associated with lower HbA(1c) value (estimates -0.008 and -0.49, P = 0.02, respectively). The structure indicators were not associated with HbA(1c), but telephone hot-line was positively associated with the process indicator BGM (estimate 4.02, P = 0.04). Children without Danish parents performed BGM significantly less frequently (-7.11, P = 0.0005) and had higher HbA(1c) (0.41, P = 0.06). CONCLUSIONS: Most process indicators were significantly associated with HbA(1c), indicating relevant action of staff on glucose regulation. The structure indicators were not associated with outcome, necessitating more detailed studies on the influence of staffing resources, treatment strategies and targets in childhood diabetes management.


Assuntos
Atenção à Saúde/normas , Diabetes Mellitus/terapia , Hemoglobinas Glicadas/análise , Adolescente , Criança , Estudos Transversais , Diabetes Mellitus/sangue , Diabetes Mellitus/patologia , Feminino , Humanos , Masculino , Avaliação de Processos e Resultados em Cuidados de Saúde , Guias de Prática Clínica como Assunto , Túnica Íntima/patologia
13.
Cleft Palate Craniofac J ; 41(4): 424-38, 2004 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-15222784

RESUMO

PURPOSE: Analysis of craniofacial morphology and growth in children with bilateral complete cleft lip and palate (BCCLP), compared with a control group with unilateral incomplete cleft lip (UICL), before any treatment as well as 20 months after lip closure. MATERIAL: The children were drawn from a group representing all Danish children with cleft born 1976 to 1981. Sixty-four children were included in the study (19 BCCLP and 45 UICL). The ages were 2 and 22 months at examinations 1 and 2, respectively. METHOD: The method of investigation was infant cephalometry in three projections. The craniofacial morphology was analyzed using linear, angular, and area variables. Growth was defined as the displacement vector from the coordinate of the corresponding landmark in the x-ray at examination 1 to its coordinate at examination 2, corrected for x-ray magnification. The growth of an anatomical region in a patient was assessed by investigating the growth pattern formed by a collection of individual growth vectors in that region. RESULTS: The BCCLP group differed significantly from the UICL group. The most striking findings in BCCLP were an extremely protruding premaxilla; markedly increased posterior maxillary width; increased width of the nasal cavity; short maxilla with reduced posterior height; short mandible; bimaxillary retrognathia; severe reduction in the size of the pharyngeal airway; and a more vertical facial growth pattern. CONCLUSION: Our findings indicate that a facial type including a wide and posterior short maxilla, short mandible, and bimaxillary retrognathia might be a liability factor that increases the probability of developing cleft lip and palate.


Assuntos
Fissura Palatina/patologia , Face/anatomia & histologia , Desenvolvimento Maxilofacial , Retrognatismo/etiologia , Estudos de Casos e Controles , Cefalometria/métodos , Fenda Labial/complicações , Fenda Labial/patologia , Fissura Palatina/complicações , Feminino , Predisposição Genética para Doença , Humanos , Lactente , Estudos Longitudinais , Masculino , Mandíbula/anormalidades , Maxila/anormalidades , Crânio/crescimento & desenvolvimento
14.
Neurology ; 62(7): 1199-201, 2004 Apr 13.
Artigo em Inglês | MEDLINE | ID: mdl-15079026

RESUMO

The authors investigated neuropsychiatric symptoms in mild cognitive impairment (MCI) from baseline data of the Investigation in the Delay to Diagnosis of AD with Exelon (InDDEx) study (n = 1,010). Neuropsychiatric symptoms were reported in 59% of subjects (Neuropsychiatric Inventory [NPI]). NPI+ subjects had significantly greater impairment on global, cognitive, and functional scores than NPI- subjects. The presence of neuropsychiatric symptoms appears to be a marker of MCI severity.


Assuntos
Doença de Alzheimer/prevenção & controle , Sintomas Comportamentais/diagnóstico , Transtornos Cognitivos/diagnóstico , Testes Neuropsicológicos/estatística & dados numéricos , Fenilcarbamatos , Idoso , Idoso de 80 Anos ou mais , Doença de Alzheimer/complicações , Doença de Alzheimer/fisiopatologia , Sintomas Comportamentais/complicações , Sintomas Comportamentais/fisiopatologia , Carbamatos/uso terapêutico , Inibidores da Colinesterase/uso terapêutico , Transtornos Cognitivos/complicações , Transtornos Cognitivos/fisiopatologia , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Rivastigmina
15.
Cleft Palate Craniofac J ; 40(4): 373-96, 2003 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-12846603

RESUMO

OBJECTIVE: Comparison of early craniofacial morphology and growth in children with nonsyndromic Robin Sequence (RS), isolated cleft palate (ICP), and unilateral complete cleft lip and palate (UCCLP). SUBJECTS: One hundred eight children with cleft: 7 with RS, 53 with ICP, and 48 with UCCLP were included in the study. The children were drawn from the group of all Danish children with cleft born 1976 through 1981. METHOD: Three-projection infant cephalometry. RESULTS: The craniofacial morphology in the RS, ICP, and UCCLP groups had some common characteristics: a wide maxilla with decreased length and posterior height, wide nasal cavity, short mandible, bimaxillary retrognathia, and reduced pharyngeal airway. The shortest mandible was found in RS followed by ICP and UCCLP; the pharyngeal airway was reduced in RS and ICP, compared with UCCLP; and the maxillary complex and nasal cavity were wider in UCCLP than in the other groups. The amount of facial growth in all three groups was similar; however, the direction was more vertical in UCCLP than in RS and ICP. CONCLUSION: Except for a shorter RS mandible, the facial morphology of infants with RS and ICP was similar, as was the amount of facial growth and the growth pattern. The differences in facial morphology can be ascribed to the difference in the primary anomaly. The amount of facial growth was similar in the three groups; however, the growth pattern showed a more vertical direction in UCCLP than in RS and ICP. It is hypothesized that the mandibular retrognathia in RS represents the outer end of that of the ICP distribution.


Assuntos
Fenda Labial/fisiopatologia , Fissura Palatina/fisiopatologia , Desenvolvimento Maxilofacial , Síndrome de Pierre Robin/fisiopatologia , Análise de Variância , Cefalometria , Feminino , Humanos , Lactente , Estudos Longitudinais , Masculino
16.
Diabet Med ; 20(7): 568-74, 2003 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-12823239

RESUMO

AIM: To describe the management of children and adolescents with Type 1 diabetes mellitus in Denmark. METHODS: Quality indicators with standards of childhood diabetes management were chosen based on international and national guidelines. Data originated from the nation-wide Danish Registry for Childhood Diabetes and two questionnaires: one questionnaire was sent to all children with diabetes (response rate 78%, n=1335) and the other was sent to the 19 centres in Denmark treating these children (response rate 100%). Simultaneously, the children were asked to take a blood sample for central HbA1c-analysis (normal range 4.3-5.8, mean 5.1%). RESULTS: Most children were managed at centres which complied with the standards for the process indicators for good diabetes management, but not with the standards for most structure and outcome indicators. Only one third of the children reached the treatment target for HbA1c. Their mean HbA1c-level increased gradually from ages 4-14 without significant difference between genders. The youngest children had the lowest HbA1c (mean 8.2%) and the lowest rate of severe hypoglycaemic events (4.6 events per 100 patient years). The subgroup of children without any hypoglycaemic events had the significantly lowest mean HbA1c-level (8.6%, P=0.028). CONCLUSIONS: The Danish Registry for Childhood Diabetes provided useful data for quality improvement, but had to be supplemented with data from questionnaires on the structure and process indicators. Outcome of paediatric diabetes management in Denmark was unsatisfactory. Centres need feedback on ways to improve care to lower the children's risk of developing severe diabetes complications.


Assuntos
Diabetes Mellitus Tipo 1/terapia , Hemoglobinas Glicadas/análise , Qualidade da Assistência à Saúde , Adolescente , Criança , Pré-Escolar , Coleta de Dados , Dinamarca , Feminino , Humanos , Masculino , Inquéritos e Questionários
17.
Cleft Palate Craniofac J ; 40(2): 131-43, 2003 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-12605518

RESUMO

PURPOSE: Craniofacial morphology and growth comparisons in children with untreated nonsyndromic Robin Sequence (RS) and a control group with unilateral incomplete cleft lip (UICL) in which the lip was surgically closed at 2 months of age. MATERIAL: The 52 children (7 RS and 45 UICL) included in the study were drawn from a group representing all Danish cleft children born 1976 through 1981. The ages of the children were 2 and 22 months at the time of examination 1 and 2, respectively. METHOD: The method of investigation was three-projection cephalometry. Craniofacial morphology was analyzed by means of linear, angular, and area variables. Growth at a specific anatomical location in a patient was defined as the displacement vector from the coordinate of the corresponding landmark at examination 1 to its coordinate at examination 2. RESULTS: The most striking findings in the RS group were markedly increased posterior maxillary width, increased width of the nasal cavity, short maxilla with reduced posterior height, short mandible, bimaxillary retrognathia, and severe reduction in size of the pharyngeal airway. The amount of facial growth was similar in the two groups; however, a tendency toward a more vertical growth direction was observed in the RS group. CONCLUSION: Facial morphology in children with RS differed significantly from that of children with UICL at both 2 and 22 months of age. The magnitude of facial growth was similar in the two groups, whereas a tendency toward a more vertical facial growth direction was observed in the RS group.


Assuntos
Fissura Palatina/fisiopatologia , Anormalidades Maxilomandibulares/fisiopatologia , Desenvolvimento Maxilofacial , Faringe/anormalidades , Síndrome de Pierre Robin/fisiopatologia , Cefalometria , Pré-Escolar , Fenda Labial/fisiopatologia , Feminino , Humanos , Lactente , Estudos Longitudinais , Masculino , Base do Crânio/anormalidades
18.
Cleft Palate Craniofac J ; 39(6): 604-22, 2002 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-12401107

RESUMO

OBJECTIVE: Analysis of craniofacial morphology and growth in children with untreated isolated cleft palate (ICP) (cleft of the secondary palate only) at 2 and 22 months of age and comparison of the morphology and growth to that of a control group with unilateral incomplete cleft lip (UICL). MATERIAL AND METHODS: A total of 98 cleft children (53 with ICP and 45 with UICL) drawn from a larger group representing all Danish children with cleft born in the period 1976 to 1981 were included in the study. Craniofacial morphology and growth were analyzed using three-projection infant cephalometry. RESULTS: The ICP group differed significantly from the UICL group. The most striking findings in the ICP group were: short maxilla; reduced posterior maxillary height; increased posterior maxillary width (in the 2-month-old); short mandible; reduced posterior height of the mandible; bimaxillary retrognathia; and reduced pharyngeal depth, height, and area. The facial growth pattern was fairly similar in the two groups except for a somewhat more vertical growth direction in the ICP group. CONCLUSION: The facial morphology in ICP children differs significantly from that of children with UICL of the same age. The differences in facial morphology can be ascribed to the difference in the primary anomaly in the ICP group. The facial growth pattern was fairly similar in the ICP and UICL group; however, a somewhat more vertical growth direction was observed in the ICP group.


Assuntos
Fenda Labial/patologia , Fissura Palatina/patologia , Face , Ossos Faciais/patologia , Desenvolvimento Maxilofacial , Crânio/patologia , Estatura , Peso Corporal , Estudos de Casos e Controles , Cefalometria , Fenda Labial/fisiopatologia , Fissura Palatina/fisiopatologia , Arco Dental/crescimento & desenvolvimento , Arco Dental/patologia , Ossos Faciais/crescimento & desenvolvimento , Feminino , Humanos , Processamento de Imagem Assistida por Computador , Lactente , Lábio/crescimento & desenvolvimento , Lábio/patologia , Estudos Longitudinais , Masculino , Mandíbula/crescimento & desenvolvimento , Mandíbula/patologia , Maxila/crescimento & desenvolvimento , Maxila/patologia , Desenvolvimento Maxilofacial/fisiologia , Nariz/crescimento & desenvolvimento , Nariz/patologia , Órbita/crescimento & desenvolvimento , Órbita/patologia , Faringe/crescimento & desenvolvimento , Faringe/patologia , Retrognatismo/patologia , Retrognatismo/fisiopatologia , Crânio/crescimento & desenvolvimento , Base do Crânio/crescimento & desenvolvimento , Base do Crânio/patologia , Estatística como Assunto , Dimensão Vertical
19.
Infect Immun ; 70(8): 4177-84, 2002 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-12117926

RESUMO

Recent data from our laboratory suggest that neutrophil granulocytes (polymorphonuclear leukocytes [PMN]) can serve as host cells for Leishmania major in the early phase of infection. In line with these findings, an early influx of PMN to the infected tissues was shown by others to be associated with susceptibility to infection with L. major. The mechanisms underlying the initial PMN recruitment to the site of infection is poorly understood. In the present study we investigated whether Leishmania can influence PMN migration. Supernatants of Leishmania promastigotes were tested for their chemotactic activity using an in vitro chemotaxis assay. All Leishmania species tested (L. major, L. aethiopica, and L. donovani) displayed a marked chemotactic effect on human PMN. However, no effect on the migration of macrophages and NK cells was observed. Checkerboard analysis revealed that the observed PMN migration was due to chemotaxis rather than chemokinesis. Most of the chemotactic activity was found in fractions containing molecules with sizes between 10 and 50 kDa. Pretreatment of PMN with N-formyl-methionyl-leucyl-phenylalanine blocked the chemotactic activity of Leishmania supernatants up to 75%. In addition, we found that leishmanial contact induced the release of interleukin-8 (IL-8) and inhibited the production of gamma interferon-inducible protein 10 (IP-10) by PMN. These data suggest that infection with Leishmania promastigotes leads to PMN accumulation via the production of a chemotactic factor by the parasites, and this effect is amplified by the induction of IL-8 production in PMN. On the other hand, the inhibition of IP-10 production can lead to prevention of NK cell activation.


Assuntos
Quimiocinas CXC/biossíntese , Fatores Quimiotáticos/imunologia , Quimiotaxia de Leucócito/imunologia , Interferon gama/imunologia , Interleucina-8/biossíntese , Leishmania/imunologia , Neutrófilos/imunologia , Adulto , Animais , Células Cultivadas , Quimiocina CXCL10 , Endopeptidase K , Calefação , Humanos , Células Matadoras Naturais/imunologia , Leishmania donovani/imunologia , Leishmania major/imunologia , Macrófagos/imunologia , Infiltração de Neutrófilos/imunologia , Neutrófilos/citologia , Receptores de Formil Peptídeo , Receptores Imunológicos/imunologia , Receptores de Peptídeos/imunologia
20.
Gesundheitswesen ; 63(12): 741-7, 2001 Dec.
Artigo em Alemão | MEDLINE | ID: mdl-11735066

RESUMO

At least in Germany social epidemiologists have practically never studied the association between the health status of children on one hand and their social status and nationality on the other. The census data from 1995 analysed here include data on social status (employment, social security, per capita income, school education) and nationality; and the 1 % sample of the population living in Germany covers all nationalities and all members of the families interviewed. The analysis includes 50,908 children aged 0-18 years and focuses on the health status and the smoking behaviour of the children and their parents. The result is somewhat surprising: In the age group 0-9 years foreign children seem to be more healthy than German children, despite the fact that their families more often belong to the lower status group and that their parents smoke more than the parents of the German children. It is hypothesised that social support in foreign families is stronger than in German families, and that this protective effect is stronger than the disadvantages of foreign children concerning social status of their families and smoking behaviour of their parents.


Assuntos
Proteção da Criança/etnologia , Comparação Transcultural , Etnicidade/estatística & dados numéricos , Indicadores Básicos de Saúde , Adolescente , Criança , Pré-Escolar , Feminino , Alemanha , Humanos , Lactente , Masculino , Fumar/efeitos adversos , Fumar/etnologia , Fatores Socioeconômicos , Poluição por Fumaça de Tabaco/efeitos adversos , Poluição por Fumaça de Tabaco/estatística & dados numéricos
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