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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Dettagli Bibliografici
Pubblicato in:Case Rep Cardiol
Autori principali: Anuwatworn, Amornpol, Sethi, Prince, Steffen, Kelly, Jonsson, Orvar, Petrasko, Marian
Natura: Artigo
Lingua:Inglês
Pubblicazione: Hindawi 2017
Soggetti:
Case Report
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC5573093/
https://ncbi.nlm.nih.gov/pubmed/28884028
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2017/1705927
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