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乳糜泻与遗传性血色素沉着症:关联及影响

Coeliac disease and hereditary haemochromatosis: association and implications.

作者信息

Singhal Amit, Moreea Sulleman, Reynolds Paul D, Bzeizi Khalid I

机构信息

Integrated Department of Gastroenterology, Bradford Teaching Hospitals NHS Trust, West Yorkshire, UK.

出版信息

Eur J Gastroenterol Hepatol. 2004 Feb;16(2):235-7. doi: 10.1097/00042737-200402000-00020.

Abstract

Coeliac disease and hereditary haemochromatosis are genetic disorders paradoxically associated with altered intestinal absorption of iron. Hereditary haemochromatosis is the most common autosomal recessive disease in the Caucasian population and is characterised by an iron overload state. Coeliac disease, or gluten sensitive enteropathy, on the other hand is frequently associated with iron deficiency anaemia. We report the cases of two patients who developed both coeliac disease and hereditary haemochromatosis. We review the literature of this rare association and examine how the clinical presentation is modified by their co-existence and the potential genetic linkage of these two disorders.

摘要

乳糜泻和遗传性血色素沉着症是与铁肠道吸收改变存在矛盾关联的遗传性疾病。遗传性血色素沉着症是白种人群中最常见的常染色体隐性疾病,其特征为铁过载状态。另一方面,乳糜泻或麸质敏感性肠病常与缺铁性贫血相关。我们报告了两名同时患乳糜泻和遗传性血色素沉着症的患者病例。我们回顾了这种罕见关联的文献,并研究了它们共存如何改变临床表现以及这两种疾病潜在的基因联系。

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