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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...
Gardado en:
| Publicado en: | Case Rep Cardiol |
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| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
Hindawi
2017
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| Assuntos: | |
| Acceso en liña: | 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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