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AB057. Wilson disease in children clinical and laboratory manifestations

BACKGROUND AND OBJECTIVE: Wilson disease (WD) is disorder of copper metabolism caused by an autosomal recessive mutation 13q14.3 in ATP7B gene. WD’s clinical manifestations are injured at liver, brain, eyes, kidneys, joints, bones, etc. which accounts for 40-50% of liver damage. The diagnosis and pr...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:Ann Transl Med
Egile Nagusiak: Van Anh, Hoang Thi, Hoa, Nguyen Pham Anh
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: AME Publishing Company 2015
Gaiak:
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC4563518/
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3978/j.issn.2305-5839.2015.AB57
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