Hemochromatosis in a β‐thalassemia minor patient with H63D homozygous mutation: A case report

β‐thalassemia heterozygosity can cause significant iron overload when accompanied by HFE gene mutations and inappropriate iron supplementation.

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Detalhes bibliográficos
Publicado no:Clin Case Rep
Main Authors: Pokhrel, Nishan Babu, Khanal, Shambhu, Chapagain, Parikshit, Pokhrel, Biraj, Shrestha, Anjan
Formato: Artigo
Idioma:Inglês
Publicado em: John Wiley and Sons Inc. 2020
Assuntos:
Case Reports
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7752352/
https://ncbi.nlm.nih.gov/pubmed/33363736
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ccr3.3096
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