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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Detalles Bibliográficos
Autores principales: Ganesh, Rajendran, Vijayakumar, Rajendran, Selvakumar, Haridoss
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2012
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3529425/
https://www.ncbi.nlm.nih.gov/pubmed/23304566
http://dx.doi.org/10.1155/2012/595343

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