| Literature DB >> 11422628 |
P J Gow1, S E Peacock, R W Chapman.
Abstract
Wilson's disease (WD) is a rare autosomal recessive disorder of copper metabolism resulting in copper-induced tissue damage that primarily involves the liver and central nervous system. The neurologic manifestations of WD almost universally involve a derangement of basal ganglia function or psychiatric disturbance. We report the case of a 46-year-old man presenting with end-stage liver disease caused by WD who had associated rapidly progressive optic neuropathy. We also discuss the possible association between the two conditions.Entities:
Mesh:
Year: 2001 PMID: 11422628 DOI: 10.1046/j.1440-1746.2001.02381.x
Source DB: PubMed Journal: J Gastroenterol Hepatol ISSN: 0815-9319 Impact factor: 4.029