Transthyretin-Related Familial Amyloid Polyneuropathy: In the Light of New Developments

Bibliographic Details
Title: Transthyretin-Related Familial Amyloid Polyneuropathy: In the Light of New Developments
Authors: Arman Çakar, Hacer Durmuş Tekçe, Feza Deymeer, Piraye Oflazer Serdaroğlu, Yeşim G Parman
Source: Türk Nöroloji Dergisi, Vol 23, Iss 3, Pp 105-111 (2017)
Publisher Information: Galenos Yayinevi, 2017.
Publication Year: 2017
Collection: LCC:Medicine
LCC:Neurology. Diseases of the nervous system
Subject Terms: Amyloidosis, transthyretin, polyneuropathy, genetics, neuropathy, Medicine, Neurology. Diseases of the nervous system, RC346-429
More Details: Transthyretin-related familial amyloid polyneuropathy (TTR-FAP) is caused by gain-of-toxic-function of TTR, which dissociates from its native tetramer form to a monomer form and aggregates in several tissues and organs. Mutations in the TTR gene lead to this amyloidogenic transformation and cause autosomal dominant disease. TTR-FAP typically causes sensorimotor FAP accompanied by autonomic involvement, but considerable phenotypic diversity is noted between different mutation types. In the event of clinical suspicion, TTR gene sequencing and pathologic confirmation are the recommended paths to follow. Significant improvement has been achieved in treating the disease over the past 20 years, starting with liver transplantation, followed by tetramer stabilizers and TTR-lowering therapies. Although there are still some uncertainties in diagnosing and treating TTR-FAP, recent advances are promising, especially in the field of treatment
Document Type: article
File Description: electronic resource
Language: English
ISSN: 1301-062X
1309-2545
Relation: http://www.tjn.org.tr/jvi.aspx?pdir=tjn&plng=eng&un=TJN-03206; https://doaj.org/toc/1301-062X; https://doaj.org/toc/1309-2545
DOI: 10.4274/tnd.03206
Access URL: https://doaj.org/article/d398437b068b4814b5b127d9d7efaa90
Accession Number: edsdoj.398437b068b4814b5b127d9d7efaa90
Database: Directory of Open Access Journals
More Details
ISSN:1301062X
13092545
DOI:10.4274/tnd.03206
Published in:Türk Nöroloji Dergisi
Language:English