Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 4 de 4
Filtrar
Mais filtros










Base de dados
Intervalo de ano de publicação
2.
Clin Exp Dermatol ; 36(2): 142-8, 2011 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-20846357

RESUMO

BACKGROUND: Keratitis-ichthyosis-deafness (KID) syndrome is a rare congenital ectodermal disorder, caused by heterozygous missense mutation in GJB2, encoding the gap junction protein connexin 26. The commonest mutation is the p.Asp50Asn mutation, and only a few other mutations have been described to date. AIM: To report the fatal clinical course and characterize the genetic background of a premature male neonate with the clinical and histological features of KID syndrome. METHODS: Genomic DNA was extracted from peripheral blood and used for PCR amplification of the GJB2 gene. Direct sequencing was used for mutation analysis. RESULTS: The clinical features included hearing impairment, ichthyosiform erythroderma with hyperkeratotic plaques, palmoplantar keratoderma, alopecia of the scalp and eyelashes, and a thick vernix caseosa-like covering of the scalp. On histological analysis, features characteristic of KID syndrome, such as acanthosis and papillomatosis of the epidermis with basket-weave hyperkeratosis, were seen. The skin symptoms were treated successfully with acitretin 0.5 mg/kg. The boy developed intraventricular and intracerebral haemorrhage, leading to hydrocephalus. His condition was further complicated by septicaemia and meningitis caused by infection with extended-spectrum beta-lactamase-producing Klebsiella pneumoniae. Severe respiratory failure followed, and the child died at 46 weeks of gestational age (13 weeks postnatally). Sequencing of the GJB2 gene showed that the child was heterozygous for a novel nucleotide change, c.263C>T, in exon 2, leading to a substitution of alanine for valine at position 88 (p.Ala88Val). CONCLUSIONS: This study has identified a new heterozygous de novo mutation in the Cx26 gene (c.263C>T; p.Ala88Val) leading to KID syndrome.


Assuntos
Conexinas/genética , Doenças do Prematuro/genética , Mutação , Animais , Biópsia , Conexina 26 , Surdez/tratamento farmacológico , Surdez/genética , Surdez/patologia , Fármacos Dermatológicos/uso terapêutico , Evolução Fatal , Humanos , Ictiose/tratamento farmacológico , Ictiose/genética , Ictiose/patologia , Recém-Nascido , Recém-Nascido Prematuro , Doenças do Prematuro/tratamento farmacológico , Doenças do Prematuro/patologia , Ceratite/tratamento farmacológico , Ceratite/genética , Ceratite/patologia , Masculino , Pele/patologia
3.
J Sch Health ; 62(2): 55-8, 1992 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-1564912

RESUMO

Women attending technical institutes often enroll in training programs for occupations with traditionally high smoking rates. In contrast, more worksites are implementing smoke-free and restricted smoking policies. "Smoking Doesn't Work," a smoking prevention project targeted at young females enrolled in a technical institute in Minnesota, used employability as the central theme in schoolwide events and classroom activities. Project intervention resulted in statistically significant increases in knowledge and awareness of smoking and employability issues. While young women enrolled in the technical institute recognized the negative image and health effects of smoking, they were less aware of the relationship between smoking status and employability. A focus on employability appears to provide a salient approach to smoking prevention with technical institute students.


Assuntos
Emprego , Educação em Saúde , Prevenção do Hábito de Fumar , Educação Vocacional , Adolescente , Adulto , Análise de Variância , Atitude Frente a Saúde , Feminino , Conhecimentos, Atitudes e Prática em Saúde , Humanos , Minnesota
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA
...