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

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

Detalles Bibliográficos
Autores principales: Pokhrel, Nishan Babu, Khanal, Shambhu, Chapagain, Parikshit, Pokhrel, Biraj, Shrestha, Anjan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Case Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7752352/
https://www.ncbi.nlm.nih.gov/pubmed/33363736
http://dx.doi.org/10.1002/ccr3.3096
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author Pokhrel, Nishan Babu
Khanal, Shambhu
Chapagain, Parikshit
Pokhrel, Biraj
Shrestha, Anjan
author_facet Pokhrel, Nishan Babu
Khanal, Shambhu
Chapagain, Parikshit
Pokhrel, Biraj
Shrestha, Anjan
author_sort Pokhrel, Nishan Babu
collection PubMed
description β‐thalassemia heterozygosity can cause significant iron overload when accompanied by HFE gene mutations and inappropriate iron supplementation.
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spelling pubmed-77523522020-12-23 Hemochromatosis in a β‐thalassemia minor patient with H63D homozygous mutation: A case report Pokhrel, Nishan Babu Khanal, Shambhu Chapagain, Parikshit Pokhrel, Biraj Shrestha, Anjan Clin Case Rep Case Reports β‐thalassemia heterozygosity can cause significant iron overload when accompanied by HFE gene mutations and inappropriate iron supplementation. John Wiley and Sons Inc. 2020-07-12 /pmc/articles/PMC7752352/ /pubmed/33363736 http://dx.doi.org/10.1002/ccr3.3096 Text en © 2020 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Reports
Pokhrel, Nishan Babu
Khanal, Shambhu
Chapagain, Parikshit
Pokhrel, Biraj
Shrestha, Anjan
Hemochromatosis in a β‐thalassemia minor patient with H63D homozygous mutation: A case report
title Hemochromatosis in a β‐thalassemia minor patient with H63D homozygous mutation: A case report
title_full Hemochromatosis in a β‐thalassemia minor patient with H63D homozygous mutation: A case report
title_fullStr Hemochromatosis in a β‐thalassemia minor patient with H63D homozygous mutation: A case report
title_full_unstemmed Hemochromatosis in a β‐thalassemia minor patient with H63D homozygous mutation: A case report
title_short Hemochromatosis in a β‐thalassemia minor patient with H63D homozygous mutation: A case report
title_sort hemochromatosis in a β‐thalassemia minor patient with h63d homozygous mutation: a case report
topic Case Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7752352/
https://www.ncbi.nlm.nih.gov/pubmed/33363736
http://dx.doi.org/10.1002/ccr3.3096
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AT chapagainparikshit hemochromatosisinabthalassemiaminorpatientwithh63dhomozygousmutationacasereport
AT pokhrelbiraj hemochromatosisinabthalassemiaminorpatientwithh63dhomozygousmutationacasereport
AT shresthaanjan hemochromatosisinabthalassemiaminorpatientwithh63dhomozygousmutationacasereport

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