• Ling-Yan Wu, Zhen-Ya Song, Qing-Hai Li, Li-Jun Mou, Ying-Ying Yu, Si-Si Shen, and Xiao-Xiao Song.
• Department of General Practice.
• Medicine (Baltimore). 2021 Apr 2; 100 (13): e25258e25258.

RationaleHereditary hemochromatosis (HH) is a hereditary disorder of iron metabolism. It is classified into 4 main types depending on the underlying genetic mutation: human hemochromatosis protein (HFE) (type 1), hemojuvelin (HJV) (type 2A), HAMP (type 2B), transferrin receptor-2 (TFER2) (type 3), and ferroportin (type 4). Type 4 HH is divided into 2 subtypes according to different mutations: type 4A (classical ferroportin disease) and type 4B (non-classical ferroportin disease). Type 4B HH is a rare autosomal dominant disease that results from mutations in the Solute Carrier Family 40 member 1 (SLC40A1) gene, which encodes the iron transport protein ferroportin.Patient ConcernsHere we report 2 elderly Chinese Han men, who were brothers, presented with liver cirrhosis, diabetes mellitus, skin hyperpigmentation, hyperferritinaemia as well as high transferrin saturation.DiagnosisSubsequent genetic analyses identified a heterozygous mutation (p. Cys326Tyr) in the SLC40A1 gene in both patients.InterventionsWe treated the patient with iron chelator and followed up for 3 years.OutcomesIron chelator helped to reduce the serum ferritin and improve the condition of target organs, including skin, pancreas, liver as well as pituitary.LessonsType 4B HH is rare but usually tends to cause multiple organ dysfunction and even death. For those patients who have difficulty tolerating phlebotomy, iron chelator might be a good alternative.Copyright © 2021 the Author(s). Published by Wolters Kluwer Health, Inc.

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