Diagnostic algorithm in transthyretin amyloidosis with cardiomyopathy
Transthyretin cardiac amyloidosis is a restrictive cardiomyopathy ((ATTR-CM), caused by an extracellular deposition of insoluble amyloid fibrils in the myocardium. It is a life threatening disease with life expectancy of 2 to 6 years after diagnosis. There are two types – hereditary and wild type. R...
Kaydedildi:
| Asıl Yazarlar: | , , , , , , , , , , , |
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| Materyal Türü: | Artigo |
| Dil: | Búlgaro |
| Baskı/Yayın Bilgisi: |
Pensoft Publishers
2020-07-01
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| Seri Bilgileri: | Българска кардиология |
| Konular: | |
| Online Erişim: | https://journal.bgcardio.org/article/53407/download/pdf/ |
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