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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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Bibliografiske detaljer
Udgivet i:Case Rep Cardiol
Main Authors: Anuwatworn, Amornpol, Sethi, Prince, Steffen, Kelly, Jonsson, Orvar, Petrasko, Marian
Format: Artigo
Sprog:Inglês
Udgivet: Hindawi 2017
Fag:
Online adgang: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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