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Hemolytic anemia as first presentation of Wilson’s disease with uncommon ATP7B mutation
Wilson’s disease (WD) is a rare inherited disorder of copper metabolism and the main manifestations are liver and brain disorders. Hemolytic anemia is an unusual complication of WD. We describe a 15-year-old girl who developed hemolytic anemia as the first manifestation of Wilson’s disease. An Arg95...
Sparad:
| I publikationen: | Int J Clin Exp Med |
|---|---|
| Huvudupphovsmän: | , , , |
| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
e-Century Publishing Corporation
2015
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| Ämnen: | |
| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4443242/ https://ncbi.nlm.nih.gov/pubmed/26064408 |
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