Literature DB >> 33363736

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

Nishan Babu Pokhrel1, Shambhu Khanal1, Parikshit Chapagain1, Biraj Pokhrel1, Anjan Shrestha2.   

Abstract

β-thalassemia heterozygosity can cause significant iron overload when accompanied by HFE gene mutations and inappropriate iron supplementation.
© 2020 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd.

Entities:  

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

Year:  2020        PMID： 33363736      PMCID： PMC7752352          DOI： 10.1002/ccr3.3096

Source DB:  PubMed          Journal:  Clin Case Rep        ISSN： 2050-0904


  1 in total

1.  Rare co-inherited alpha-thalassemia minor and beta-thalassemia minor with heterozygous H63D mutation mistaken as iron deficiency anemia: a case report.

Authors:  Arooj Fatima Chaudhry; Zulfiqar Malik; Cameron Joseph Shegos
Journal:  AME Case Rep       Date:  2022-01-25
  1 in total

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