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Hereditary cardiac amyloidosis associated with Pro24Ser transthyretin mutation: a case report
BACKGROUND: Transthyretin amyloidosis is a systemic disorder caused by extracellular deposition of insoluble amyloid fibrils in peripheral and autonomic nerves, heart, kidney, gastrointestinal tract, and other organs. Hereditary transthyretin amyloidosis is an autosomal dominant disease. More than 1...
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| Publicado no: | J Med Case Rep |
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| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6295314/ https://ncbi.nlm.nih.gov/pubmed/30553273 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13256-018-1931-5 |
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