Síndrome de Marfan e Dissecção Carotídea Bilateral

Autores

  • Roberto Magalhães Carneiro de Oliveira

DOI:

https://doi.org/10.34024/rnc.1999.v7.10319

Palavras-chave:

Síndrome de Marfan, dissecção arterial

Resumo

A síndrome de Marfan é uma doença do tecido conectivo de herança autossômica dominante, que afeta os ossos, os olhos, os pulmões e o sistema cardiovascular. Relatamos o caso de um rapaz de 16 anos com síndrome de Marfan que apresentou infarto frontoparietal direito. A angiografia cerebral mostrou oclusão de artéria carótida interna esquerda e estenose da artéria carótida interna direita, com padrão de dissecção próximo à sua origem. Ressaltamos a importância de se investigar doenças do tecido conjuntivo em pacientes jovens com dissecção arterial mesmo na ausência de história familiar.

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Publicado

1999-09-30

Como Citar

Oliveira, R. M. C. de. (1999). Síndrome de Marfan e Dissecção Carotídea Bilateral . Revista Neurociências, 7(3), 145–148. https://doi.org/10.34024/rnc.1999.v7.10319

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