An Unusual Case of Hemochromatosis in an African-American Man: Case Report and Review of the Literature

被引:0
|
作者
David A. Labowitz
Jennifer Bontreger
Albert D. Min
机构
[1] Beth Israel Medical Center,Department of Medicine
来源
Digestive Diseases and Sciences | 2007年 / 52卷
关键词
Iron Overload; Hemochromatosis; Transferrin Saturation; Hereditary Hemochromatosis; Northern European Descent;
D O I
暂无
中图分类号
学科分类号
摘要
引用
收藏
页码:3519 / 3520
页数:1
相关论文
共 50 条
  • [21] Hemochromatosis, alcoholism and unhealthy dietary fat: a case report
    Venkatachalam Shobi
    Awe Adeseye
    Ballard Billy
    Kalliny Medhat
    Journal of Medical Case Reports, 15
  • [22] Case report: Arthropathy as the presenting symptom in hereditary hemochromatosis
    Tanglao, EC
    Stern, MA
    Agudelo, CA
    AMERICAN JOURNAL OF THE MEDICAL SCIENCES, 1996, 312 (06) : 306 - 309
  • [23] Hemochromatosis in India: First Report of Whole Exome Sequencing With Review of the Literature
    Koshy, Abraham
    Mukkada, Roy J.
    Chettupuzha, Antony P.
    Francis, Jose, V
    Kandathil, Julio C.
    Mahadevan, Pushpa
    JOURNAL OF CLINICAL AND EXPERIMENTAL HEPATOLOGY, 2020, 10 (02) : 163 - 169
  • [24] An aviator with cardiomyopathy and genetic susceptibility to hereditary hemochromatosis: A case report
    Hanson, EH
    Shue, PM
    Palm-Leis, A
    Rowley, RK
    AVIATION SPACE AND ENVIRONMENTAL MEDICINE, 2001, 72 (10): : 924 - 927
  • [25] Hemochromatosis as a secondary condition to systemic lupus erythematosus: A case report
    Liu, Jun
    Zeng, Jiashun
    Li, Peiting
    Li, Long
    Gao, Xueqin
    INTERNATIONAL JOURNAL OF RHEUMATIC DISEASES, 2023, 26 (11) : 2297 - 2300
  • [26] Homozygous form of hereditary hemochromatosis in a patient with beta-thalassemia minor: case report
    Buljubasic, Dunja
    Ladenhauser-Palijan, Tatjana
    Debelijak, Zeljko
    BIOCHEMIA MEDICA, 2009, 19 (02) : 199 - 205
  • [27] Roxadustat and transfusional iron overload induced hypothyroidism in a hemodialysis patient: a case report with a literature review
    Yamashita, Chikako
    Hirai, Yuri
    Nishigaito, Toshiya
    Mitsumoto, Kensuke
    Mizumoto, Aya
    Kawakami, Manabu
    Uzu, Takashi
    RENAL REPLACEMENT THERAPY, 2024, 10 (01)
  • [28] Case report: A rare case of hereditary hemochromatosis caused by a mutation in the HAMP gene in Fuyang, China
    Wang, Jinling
    Xu, Jing
    Jiang, Ning
    Liu, Hui
    Li, Fengcheng
    Wang, Beibei
    Wang, Jin
    Chu, Ziyu
    Tan, Lin
    Li, Shasha
    FRONTIERS IN MEDICINE, 2024, 11
  • [29] Hemochromatosis in a β-thalassemia minor patient with H63D homozygous mutation: A case report
    Pokhrel, Nishan Babu
    Khanal, Shambhu
    Chapagain, Parikshit
    Pokhrel, Biraj
    Shrestha, Anjan
    CLINICAL CASE REPORTS, 2020, 8 (12): : 2341 - 2345
  • [30] A Novel Mutation of Transferrin Receptor 2 in a Chinese Pedigree With Type 3 Hemochromatosis: A Case Report
    Tang, Shan
    Bai, Li
    Gao, Yuan
    Hou, Wei
    Song, Wenyan
    Liu, Hui
    Hu, Zhongjie
    Duan, Zhongping
    Zhang, Liaoyun
    Zheng, Sujun
    FRONTIERS IN GENETICS, 2022, 13