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

Clinical Case Reports

Anjan Shrestha¹  Nishan Babu Pokhrel²  Shambhu Khanal²  Biraj Pokhrel²  Parikshit Chapagain² 

[1] Department of Hemato‐Oncology Tribhuvan University Institute of Medicine Kathmandu Nepal;Department of Internal Medicine Tribhuvan University Institute of Medicine Kathmandu Nepal;

关键词: anemia;    h63d mutation;    hereditary hemochromatosis;    HFE gene;    iron overload;    β‐thalassemia;   

DOI  :  10.1002/ccr3.3096

来源: DOAJ

【 摘 要 】

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

【 授权许可】

Unknown