期刊论文详细信息
Clinical Case Reports
Hemochromatosis in a β‐thalassemia minor patient with H63D homozygous mutation: A case report
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   

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