Hemochromatosis in a β‐thalassemia minor patient with H63D homozygous mutation: A case report
oleh: Nishan Babu Pokhrel, Shambhu Khanal, Parikshit Chapagain, Biraj Pokhrel, Anjan Shrestha
| Format: | Article |
|---|---|
| Diterbitkan: | Wiley 2020-12-01 |
Deskripsi
Abstract β‐thalassemia heterozygosity can cause significant iron overload when accompanied by HFE gene mutations and inappropriate iron supplementation.