Wilson disease

Wilson disease is a very rare inherited multisystemic disease presenting non-specific neurological, hepatic, psychiatric or osseo-muscular manifestations due to excessive copper deposition in the body.

Vomiting

Forceful ejection of the contents of the stomach through the mouth by means of a series of involuntary spasmic contractions.


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PMID (PMCID)
29914392
(6006946)
 MIXED_SAMPLE Child
Three novel mutations in the ATP7B gene of unrelated Vietnamese patients with Wilson disease.
Huong NTM, Lien NTK, Ngoc ND, Mai NTP, Hoa NPA, Hai LT, Van Chi P, Van TT, Van Khanh T, Hoang NH.
BMC Med Genet. 2018;19(1):104.
These patients had clinical features such as numbness of hands and feet, vomiting, insomnia, palsy, liver failure and Kayser-Fleischer (K-F) rings and were diagnosed with Wilson disease in the Human Genetics Department, Vietnam National Children's Hospital.