Orthopaedic Aspects of Marfan Syndrome: The Experience of a Referral Center for Diagnosis of Rare Diseases

Marfan syndrome is caused by mutations in the fibrillin-1 gene (FBN1). The most important features affect the cardiovascular system, eyes, and skeleton. The aim of this study was to report the most frequent musculoskeletal alterations observed in 146 patients affected by Marfan syndrome. Fifty-four...

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Detalles Bibliográficos
Autores principales: De Maio, Fernando, Fichera, Alessandro, De Luna, Vincenzo, Mancini, Federico, Caterini, Roberto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2016
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5165130/
https://www.ncbi.nlm.nih.gov/pubmed/28050285
http://dx.doi.org/10.1155/2016/8275391

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5165130/
https://www.ncbi.nlm.nih.gov/pubmed/28050285
http://dx.doi.org/10.1155/2016/8275391

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