[Hemochromatosis - too much iron].

Deutsche medizinische Wochenschrift (1946) Pub Date : 2024-10-01 Epub Date: 2024-10-09 DOI:10.1055/a-2279-8279
Lorenz Michael Pammer, Benedikt Schäfer
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Abstract

Hemochromatosis is a disorder of genetic origin which affects iron hemostasis, resulting in an increased transferrin saturation, hyperferritinemia and parenchymal iron overload.Recently, a new system for the classification of hemochromatosis has been proposed, wherein patients are separated into 4 groups, based on the disease affected iron regulatory genes. Excess iron and increased transferrin saturation results in the formation of non-transferrin bound iron which leads to tissue damage. Hemochromatosis is a common genetic disease, but screening of the general population is not routinely recommended. In order to provide ideal care for hemochromatosis patients, it is crucial to delineate hemochromatosis from other causes of hyperferritinemia, which is a common finding in patients with metabolic disorders. This article summarizes the diagnostic algorithm for hemochromatosis. Furthermore, recommendations for optimal care - including targets for phlebotomy - are discussed.

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[血色沉着病--铁过多]。
血色沉着病是一种遗传性疾病,会影响铁的止血功能,导致转铁蛋白饱和度升高、高铁蛋白血症和实质铁超载。最近,有人提出了一套新的血色沉着病分类系统,根据受疾病影响的铁调节基因,将患者分为 4 组。铁过量和转铁蛋白饱和度升高会形成非转铁蛋白结合铁,从而导致组织损伤。血色沉着病是一种常见的遗传疾病,但并不建议对普通人群进行常规筛查。为了给血色沉着症患者提供理想的治疗,必须将血色沉着症与其他原因导致的高铁蛋白血症区分开来,因为高铁蛋白血症是代谢紊乱患者的常见病。本文总结了血色病的诊断算法。此外,还讨论了最佳护理建议,包括抽血检查的目标。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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