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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...
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| Vydáno v: | Ann Transl Med |
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| Hlavní autoři: | , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
AME Publishing Company
2015
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| Témata: | |
| On-line přístup: | 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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