Diagnosis and management of transthyretin familial amyloid polyneuropathy in Japan: red-flag symptom clusters and treatment algorithm

Hereditary ATTR (ATTRm) amyloidosis (also called transthyretin-type familial amyloid polyneuropathy [ATTR-FAP]) is an autosomal-dominant, adult-onset, rare systemic disorder predominantly characterized by irreversible, progressive, and persistent peripheral nerve damage. TTR gene mutations (e.g. rep...

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Spremljeno u:
Bibliografski detalji
Izdano u:Orphanet J Rare Dis
Glavni autori: Sekijima, Yoshiki, Ueda, Mitsuharu, Koike, Haruki, Misawa, Sonoko, Ishii, Tomonori, Ando, Yukio
Format: Artigo
Jezik:Inglês
Izdano: BioMed Central 2018
Teme:
Review
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC5773042/
https://ncbi.nlm.nih.gov/pubmed/29343286
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13023-017-0726-x
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