دورية أكاديمية

Hereditary hemochromatosis caused by a C282Y/H63D mutation in the HFE gene: A case report

التفاصيل البيبلوغرافية
العنوان: Hereditary hemochromatosis caused by a C282Y/H63D mutation in the HFE gene: A case report
المؤلفون: Dongdong Li, Jinfeng Li, Hongkun Zhang, Qiuyu Zhu, Teng Wang, Wen Zhao, Shousong Zhao, Wei Li
المصدر: Heliyon, Vol 10, Iss 7, Pp e28046- (2024)
بيانات النشر: Elsevier, 2024.
سنة النشر: 2024
المجموعة: LCC:Science (General)
LCC:Social sciences (General)
مصطلحات موضوعية: Hereditary hemochromatosis (HH), HFE gene, C282Y/H63D, Science (General), Q1-390, Social sciences (General), H1-99
الوصف: Hereditary hemochromatosis (HH) is a disease characterized by disordered iron metabolism. It often involves mutations of the HFE gene, which encodes the homeostatic iron regulator protein (HFE), as well as mutations affecting hepcidin antimicrobial peptide, hemojuvelin, or transferrin receptor 2. Historically, HH has been observed primarily in European and European diaspora populations, while classical HH is rare in Asian populations, including in China. In this article, we report a rare case of HH in a Chinese man that could be attributed to a heterozygous C282Y/H63D HFE mutation. Based on clinical examination, liver biopsy, and genetic testing results, the patient was diagnosed with HH. Clinical signs and symptoms and serum iron-related test results were recorded for a period of two years after the patient began treatment. Over this observation period, the patient was subjected to 25 phlebotomies (accounting for a total blood loss of 10.2 L). His serum ferritin levels decreased from 1550 μg/L to 454 μg/L, his serum iron concentration decreased from 40 μmol/L to 24.6 μmol/L, and his transferrin saturation decreased from 97.5% to 55.1%. Early diagnosis is essential for patients with HH to obtain good outcomes. Regular phlebotomy after diagnosis can improve HH symptoms and delay HH disease progression.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 2405-8440
العلاقة: http://www.sciencedirect.com/science/article/pii/S2405844024040775Test; https://doaj.org/toc/2405-8440Test
DOI: 10.1016/j.heliyon.2024.e28046
الوصول الحر: https://doaj.org/article/8e3b989d153347dd8b5c551cca12d8b2Test
رقم الانضمام: edsdoj.8e3b989d153347dd8b5c551cca12d8b2
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:24058440
DOI:10.1016/j.heliyon.2024.e28046