Isolated infrarenal abdominal aorta aneurysm in a 42-year-old patient with Marfan’s syndrome: Case report

Marfan’s syndrome is an autosomal dominant disorder of connective tissue characterized by a large number of possible mutations and by heterogeneity of clinical presentation primarily in skeletal, ocular and cardiovascular organ systems. Cardiovascular complications of the disease are responsible for...

Descripción completa

Detalles Bibliográficos
Autores principales: Jiber, Hamid, Hajji, Rita, Zrihni, Youssef, Zaghloul, Rachid, Zizi, Othman, Bouarhroum, Abdellatif
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2013
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4857274/
https://www.ncbi.nlm.nih.gov/pubmed/27489631
http://dx.doi.org/10.1177/2050313X13507564

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4857274/
https://www.ncbi.nlm.nih.gov/pubmed/27489631
http://dx.doi.org/10.1177/2050313X13507564

Ejemplares similares