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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Detalles Bibliográficos
Autores principales: Yamamoto, Hiroyuki, Hashimoto, Toru, Kawamura, Shunji, Hiroe, Michiaki, Yamashita, Taro, Ando, Yukio, Yokochi, Tomoki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6295314/
https://www.ncbi.nlm.nih.gov/pubmed/30553273
http://dx.doi.org/10.1186/s13256-018-1931-5

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