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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Detalles Bibliográficos
Autores principales: Lescano, Manuel A, Tavares, Letícia C, Santos, Paulo C J L
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2017
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5649000/
https://www.ncbi.nlm.nih.gov/pubmed/29085829
http://dx.doi.org/10.12998/wjcc.v5.i10.381

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5649000/
https://www.ncbi.nlm.nih.gov/pubmed/29085829
http://dx.doi.org/10.12998/wjcc.v5.i10.381

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