Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 2 de 2
Filtrar
Adicionar filtros








Intervalo de ano
1.
Arch. cardiol. Méx ; 76(4): 448-453, oct.-dic. 2006.
Artigo em Espanhol | LILACS | ID: lil-568602

RESUMO

A case of Williams' syndrome in a 22 years old man, is described. Clinical data, as well as those of laboratory and of imageneology study, are reported. An electro-anatomical comparison permitted to verify the value of electrocardiographic signs of enlargement of the four heart chambers, due to a mixed overload. It permitted also to establish the value of the signs of the interatrial block, probably due to myocardial atrial fibrosis, and those suggesting hyperkalemia. The electrocardiogram always is very useful because it furnishes certain functional aspects permitting to allow structural inferences, in following subjects with congenital or acquired heart diseases.


Assuntos
Adulto , Humanos , Masculino , Eletroencefalografia , Síndrome de Williams , Síndrome de Williams/patologia , Autopsia , Aorta Abdominal/patologia , Aorta Torácica/patologia , Aorta/patologia , Átrios do Coração/patologia , Ventrículos do Coração/patologia , Insuficiência da Valva Mitral/patologia , Valva Mitral/patologia , Artéria Pulmonar/patologia , Síndrome de Williams/mortalidade , Síndrome de Williams
2.
Rev. Soc. Cardiol. Estado de Säo Paulo ; 11(6): 1033-1043, nov.-dez. 2001. ilus
Artigo em Inglês | LILACS | ID: lil-391571

RESUMO

The elastic property of several tissues is conferred by the elastic fiber, composed of a homogeneous core of elastin surrounded by microfibrils. Defects in these components lead to different genetic diseases with important cardiovascular manifestations in the aorta. Here we will review these genetic disorders associated with pathologies of the aorta, focusing on the molecular defects underlying them, and on how the elucidation of the molecular lesion can lead to a better understanding of disease progression. In particular, we will discuss the recent advances in the molecular basis of supravalvar aortic stenosis, Williams syndrome, Marfan syndrome, and the fibrillinopathies.


Assuntos
Humanos , Masculino , Feminino , Camundongos , Estenose Aórtica Supravalvular/congênito , Estenose Aórtica Supravalvular/diagnóstico , Estenose Aórtica Supravalvular/patologia , Síndrome de Marfan/diagnóstico , Síndrome de Marfan/genética , Síndrome de Marfan/patologia , Síndrome de Williams/diagnóstico , Síndrome de Williams/epidemiologia , Síndrome de Williams/patologia , Aorta , Aneurisma Aórtico , Dissecação , Elastina , Doenças Genéticas Inatas , Genética , Fenótipo , Fatores de Tempo
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA