| Literature DB >> 30365625 |
Marcus Vinicius Pinto1, Amilton Antunes Barreira2, Acary Souza Bulle3, Marcos Raimundo Gomes de Freitas1, Marcondes Cavalcante França4, Francisco de Assis Aquino Gondim5,6, Carlo Domenico Marrone7, Wilson Marques2, Osvaldo J M Nascimento8, Francisco Tellechea Rotta9, Camila Pupe8, Márcia Waddington-Cruz1.
Abstract
Transthyretin familial amyloid polyneuropathy is an autosomal dominant inherited sensorimotor and autonomic polyneuropathy, which if untreated, leads to death in approximately 10 years. In Brazil, liver transplant and tafamidis are the only disease-modifying treatments available. This review consists of a consensus for the diagnosis, management and treatment for transthyretin familial amyloid polyneuropathy from the Peripheral Neuropathy Scientific Department of the Brazilian Academy of Neurology. The first and last authors produced a draft summarizing the main views on the subject and emailed the text to 10 other specialists. Relevant literature on this subject was reviewed by each participant and used for the individual review of the whole text. Each participant was expected to review the text and send a feedback review by e-mail. Thereafter, the 12 panelists got together at the city of Fortaleza, discussed the controversial points, and reached a consensus for the final text.Entities:
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Year: 2018 PMID: 30365625 DOI: 10.1590/0004-282X20180094
Source DB: PubMed Journal: Arq Neuropsiquiatr ISSN: 0004-282X Impact factor: 1.420