Anomalous Coronary Artery Origin in a Young Patient with Marfan Syndrome

Marfan syndrome is an autosomal dominant genetic disorder that affects connective tissue and is caused by mutations in the fibrillin 1 gene present at chromosome 15. Aortic aneurysm is its main complication, and along the dilation of the aorta root and its descending portion (60–100%), with secondar...

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Detalles Bibliográficos
Autores principales: Duarte, S. B. C. P., Beraldo, D. O., Cesar, L. A. M., Mansur, A. P., Takada, J. Y.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2017
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5752982/
https://www.ncbi.nlm.nih.gov/pubmed/29430308
http://dx.doi.org/10.1155/2017/3861923

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5752982/
https://www.ncbi.nlm.nih.gov/pubmed/29430308
http://dx.doi.org/10.1155/2017/3861923

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