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










Base de dados
Intervalo de ano de publicação
1.
BMJ Case Rep ; 20152015 Feb 25.
Artigo em Inglês | MEDLINE | ID: mdl-25716036

RESUMO

Noonan syndrome is an autosomal dominant disorder with genetically heterogeneous inheritance. The incidence of cardiac abnormalities is higher in patients with Noonan syndrome and approximately 80% patients with Noonan syndrome are reported to have cardiac abnormalities during their lifetimes. However, polyvalvular disease in Noonan syndrome is rare. In this case-report, we describe a case of a young man whose features were strongly suggestive of Noonan syndrome and who was diagnosed with prolapse of all four cardiac valves after 22 years of uneventful survival.


Assuntos
Anormalidades Múltiplas/genética , Cardiopatias Congênitas/genética , Prolapso das Valvas Cardíacas/genética , Síndrome de Noonan/genética , Anormalidades Múltiplas/diagnóstico , Adulto , Diagnóstico Diferencial , Face/anormalidades , Cardiopatias Congênitas/diagnóstico , Prolapso das Valvas Cardíacas/diagnóstico , Humanos , Deficiência Intelectual/genética , Masculino , Síndrome de Noonan/diagnóstico
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA
...