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Marfan Syndrome: A Case Report

Marfan syndrome is an autosomal dominant systemic disorder of the connective tissue. Children affected by the Marfan syndrome carry a mutation in one of their two copies of the gene that encodes the connective tissue protein fibrillin-1. Marfan syndrome affects most organs and tissues, especially th...

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Detalhes bibliográficos
Main Authors: Ganesh, Rajendran, Vijayakumar, Rajendran, Selvakumar, Haridoss
Formato: Artigo
Idioma:Inglês
Publicado em: Hindawi Publishing Corporation 2012
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3529425/
https://ncbi.nlm.nih.gov/pubmed/23304566
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2012/595343
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