Ala97Ser transthyretin amyloidosis-associated polyneuropathy, clinical and neurophysiological profiles in a Thai cohort

Ala97Ser transthyretin amyloidosis-associated polyneuropathy, clinical and neurophysiological profiles in a Thai cohort

Abstract Background Ala97Ser transthyretin amyloidosis-associated polyneuropathy (ATTRA97S-PN) is a rare form of inherited polyneuropathy, usually manifesting with late-onset (> 50) progressive polyneuropathy. This mutation is mostly prevalent in Taiwanese and Han-Chinese individuals. The aim of...

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Bibliographic Details
Main Authors: Nath Pasutharnchat, Chamaiporn Taychargumpoo, Yongkasem Vorasettakarnkij, Jakkrit Amornvit
Format: Article
Language:English
Published: BMC 2021-05-01
Series:BMC Neurology
Subjects:
hereditary transthyretin amyloidosis-associated polyneuropathy
transthyretin
Ala97Ser
Thais
neurophysiological study
autonomic neuropathy
Online Access:https://doi.org/10.1186/s12883-021-02243-3

Internet

https://doi.org/10.1186/s12883-021-02243-3

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