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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Vydáno v:Orphanet J Rare Dis
Hlavní autoři: Sekijima, Yoshiki, Ueda, Mitsuharu, Koike, Haruki, Misawa, Sonoko, Ishii, Tomonori, Ando, Yukio
Médium: Artigo
Jazyk:Inglês
Vydáno: BioMed Central 2018
Témata:
Review
On-line přístup: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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