Wilson's disease
English
Etymology
Named after Samuel Alexander Kinnier Wilson (1878–1937), the British neurologist who first described the condition in 1912.
Proper noun
- (medicine) An autosomal-recessive genetic disorder in which copper accumulates in tissues, resulting in neurological or psychiatric symptoms and liver disease.
- Synonym: hepatolenticular degeneration
Translations
autosomal-recessive genetic disorder
|
See also
This article is issued from Wiktionary. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.