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

Nishan Babu Pokhrel; Shambhu Khanal; Parikshit Chapagain; Biraj Pokhrel; Anjan Shrestha

Journal ArticleOPEN ACCESS

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

Pokhrel N
Khanal S
Chapagain P
et al.

Clinical Case Reports (2020) 8(12) 2341-2345

DOI: 10.1002/ccr3.3096

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Abstract

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

Author supplied keywords

HFE gene
anemia
h63d mutation
hereditary hemochromatosis
iron overload
β-thalassemia

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CITATION STYLE

APA

Pokhrel, N. B., Khanal, S., Chapagain, P., Pokhrel, B., & Shrestha, A. (2020). Hemochromatosis in a β-thalassemia minor patient with H63D homozygous mutation: A case report. Clinical Case Reports, 8(12), 2341–2345. https://doi.org/10.1002/ccr3.3096

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

Abstract

Author supplied keywords

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