Late-onset Hemochromatosis: Co-inheritance of β-thalassemia and Hereditary Hemochromatosis in a Chinese Family: A Case Report and Epidemiological Analysis of Diverse Populations
Author:
Affiliation:
1. Department of Hematology and Hematology Research Laboratory, West China Hospital, Sichuan University, China
2. Division of Molecular Bioregulation, Cancer Research Institute, Kanazawa University, Japan
Publisher
Japanese Society of Internal Medicine
Subject
General Medicine,Internal Medicine
Link
https://www.jstage.jst.go.jp/article/internalmedicine/57/23/57_8628-16/_pdf
Reference34 articles.
1. 1. Merryweather-Clarke AT, Pointon JJ, Shearman JD, et al. Global prevalence of putative haemochromatosis mutations. J Med Genet 34: 275-278, 1997.
2. 2. Hanson EH, Imperatore G, Burke W. HFE gene and hereditary hemochromatosis: a HuGE review. Human Genome Epidemiology. Am J Epidemiol 154: 193-206, 2001.
3. 3. Franchini M. Hereditary iron overload: update on pathophysiology, diagnosis, and treatment. Am J Hematol 81: 202-209, 2006.
4. 4. Zhou WX, Wu XR, Bennett AE, et al. Endoscopic and histologic abnormalities of gastrointestinal tract in patients with hereditary hemochromatosis. J Clin Gastroenterol 48: 336-342, 2014.
5. 5. Weatherall DJ, Clegg JB. The β Thalassemias.4nd edn ed. Blackwell Science Ltd, 2008.
Cited by 6 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. The Exploring of Growth Differentiation Factor-15 and H63D Gene Polymorphisms in β-thalassemia Major: Implications for Cardiovascular Risk and Iron Overload;Journal of Applied Hematology;2024-01
2. Comparison between H63D and G71D gene mutation effects on iron overload in Iraqi patients with β-thalassemia major: A case–control study;Iraqi Journal of Hematology;2022
3. Rare co-inherited alpha-thalassemia minor and beta-thalassemia minor with heterozygous H63D mutation mistaken as iron deficiency anemia: a case report;AME Case Reports;2022-01
4. Association of HFE Gene Mutations With Serum Ferritin Level and Heart and Liver Iron Overload in Patients With Transfusion-dependent Beta-Thalassemia;Journal of Pediatric Hematology/Oncology;2020-09-11
5. Hemochromatosis in a β‐thalassemia minor patient with H63D homozygous mutation: A case report;Clinical Case Reports;2020-07-12
1.学者识别学者识别
2.学术分析学术分析
3.人才评估人才评估
"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370
www.globalauthorid.com
TOP
Copyright © 2019-2024 北京同舟云网络信息技术有限公司 京公网安备11010802033243号 京ICP备18003416号-3