Literature DB >> 30365625

Brazilian consensus for diagnosis, management and treatment of transthyretin familial amyloid polyneuropathy.

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.

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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


  1 in total

1.  Patient-reported outcomes on familial amyloid polyneuropathy (FAP).

Authors:  Fabian J Bolte; Christel Langenstroer; Frauke Friebel; Anna Hüsing-Kabar; Martin Dugas; Hartmut H Schmidt
Journal:  Orphanet J Rare Dis       Date:  2020-10-14       Impact factor: 4.123

  1 in total

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