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

Internet

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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