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

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

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

Bibliographic Details
Main Authors: Nishan Babu Pokhrel, Shambhu Khanal, Parikshit Chapagain, Biraj Pokhrel, Anjan Shrestha
Format: Article
Language:English
Published: Wiley 2020-12-01
Series:Clinical Case Reports
Subjects:
anemia
h63d mutation
hereditary hemochromatosis
HFE gene
iron overload
β‐thalassemia
Online Access:https://doi.org/10.1002/ccr3.3096

Internet

https://doi.org/10.1002/ccr3.3096

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