Spontaneous Coronary Artery Dissection: A Rare Manifestation of Alport Syndrome

Alport syndrome (AS) is a genetic disorder due to inheritance of genetic mutations which lead to production of abnormal type IV collagen. AS has been associated with renal, auditory, and ocular diseases due to the presence of abnormal alpha chains of type IV collagen in the glomerulus, cochlea, corn...

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Detalles Bibliográficos
Autores principales: Anuwatworn, Amornpol, Sethi, Prince, Steffen, Kelly, Jonsson, Orvar, Petrasko, Marian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2017
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5573093/
https://www.ncbi.nlm.nih.gov/pubmed/28884028
http://dx.doi.org/10.1155/2017/1705927

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5573093/
https://www.ncbi.nlm.nih.gov/pubmed/28884028
http://dx.doi.org/10.1155/2017/1705927

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