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Juvenile hemochromatosis: HAMP mutation and severe iron overload treated with phlebotomies and deferasirox
Juvenile hemochromatosis (JH) is a rare condition classified as an autosomal recessive disorder that leads to severe iron absorption. JH usually affects people under the age of 30 and presents symptoms such as chronic liver damage, hypogonadotropic hypogonadism, cardiac diseases and endocrine dysfun...
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| Gepubliceerd in: | World J Clin Cases |
|---|---|
| Hoofdauteurs: | , , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
Baishideng Publishing Group Inc
2017
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5649000/ https://ncbi.nlm.nih.gov/pubmed/29085829 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.12998/wjcc.v5.i10.381 |
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