NDLI: A brief communication of patients with homozygous C282Y mutation-related hereditary hemochromatosis

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A brief communication of patients with homozygous C282Y mutation-related hereditary hemochromatosis

Content Provider	Europe PMC
Author	Gokcan, Hale Oz, Didem Kuru Bodakci, Emin Tunc, Esra Idilman, Ramazan
Abstract	Hereditary hemochromatosis (HH) is an autosomal recessive inherited iron-loading disorder and is characterized by chronic hepatitis, cirrhosis, diabetes, and bronze skin. The hemochromatosis gene (C282Y homozygosity)-related hemochromatosis is the most common form of HH. The prevalence of HH is varied. Here, we defined six cases with C282Y homozygosity-related HH in a single center in Turkiye.
Related Links	https://europepmc.org/backend/ptpmcrender.fcgi?accid=PMC11237243&blobtype=pdf
ISSN	13075888
Volume Number	5
DOI	10.14744/hf.2024.2024.0020
PubMed Central reference number	PMC11237243
Issue Number	3
PubMed reference number	PMC11237243
Journal	Hepatology Forum [Hepatol Forum]
e-ISSN	27577392
Language	English
Publisher	Kare Publishing
Publisher Date	2024-01-01
Publisher Place	Turkey
Access Restriction	Open
Rights License	This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License (CC BY-NC 4.0)
Subject Keyword	C282 Y homozygous mutation hereditary hemochromatosis HFE gene
Content Type	Text
Resource Type	Article
Subject	Hepatology Gastroenterology

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