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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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| Publicado no: | Ann Transl Med |
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| Main Authors: | , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
AME Publishing Company
2015
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| Assuntos: | |
| Acesso em linha: | 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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