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

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

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_11237243

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

About this item

Full title

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

Publisher

Turkey: Kare Publishing

Journal title

Hepatology forum, 2024-07, Vol.5 (3), p.161-164

Language

English

Formats

Publication information

Publisher

Turkey: Kare Publishing

Subjects

Subjects and topics

More information

Scope and Contents

Contents

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 homozygo...

Alternative Titles

Full title

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

Authors, Artists and Contributors

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_11237243

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_11237243

Other Identifiers

ISSN

2757-7392,1307-5888

E-ISSN

2757-7392

DOI

10.14744/hf.2024.2024.0020

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