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559 CNS impairment in the children from patients with Wilson disease

✍ Scribed by R. Bruha; Z. Marecek; P. Martasek; S. Nevsimalova; J. Petrtyl; P. Urbanek

Book ID: 117373387
Publisher: Elsevier Science
Year: 2004
Tongue: English
Weight: 60 KB
Volume: 40
Category: Article
ISSN: 0168-8278
DOI: 10.1016/s0168-8278(04)90559-4

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## Abstract Wilson's disease (WD) is an inherited autosomal‐recessive disorder of copper metabolism characterized by a wide variety of neurological, hepatic, and psychiatric symptoms. The aim of the present study was the development and evaluation of a clinical rating scale, termed Unified Wilson's