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A brief communication of patients with homozygous C282Y mutation-related hereditary hemochromatosis.
Hepatol Forum
; 5(3): 161-164, 2024.
Artículo
en Inglés
| MEDLINE
| ID: mdl-39006143
RESUMEN
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.