Wilson disease: the diagnostic challenge and treatment outcomes in a series of 262 cases

Wilson disease: the diagnostic challenge and treatment outcomes in a series of 262 cases

Background Wilson disease (WD) is an autosomal recessive disorder that leads to organ toxicity due to copper overload. Early diagnosis is complicated by the rarity and diversity of manifestations.

Saved in:

Bibliographic Details
Main Authors:	Marta Mitiko Deguti, Fabiana Cordeiro Araujo, Débora Raquel Benedita Terrabuio, Thiago Ferreira Araujo, Egberto Reis Barbosa, Gilda Porta, Eduardo Luiz Rachid Cançado
Format:	Article
Language:	English
Published:	Thieme Revinter Publicações 2024-05-01
Series:	Arquivos de Neuro-Psiquiatria
Subjects:	Hepatolenticular Degeneration Copper-Transporting ATPases Movement Disorders Penicillamine Liver Cirrhosis Degeneração Hepatolenticular ATPases Transportadoras de Cobre Transtornos dos Movimentos Penicilamina Cirrose Hepática
Online Access:	http://www.thieme-connect.de/DOI/DOI?10.1055/s-0044-1786855
Tags:	Add Tag No Tags, Be the first to tag this record!

Internet

http://www.thieme-connect.de/DOI/DOI?10.1055/s-0044-1786855