在血色素沉着症基因被发现后重新审视各种铁过载综合征。
Revisiting various iron overload syndromes after the haemochromatosis gene discovery.
作者信息
Worwood M
机构信息
Department of Haematology, University of Wales College of Medicine, Cardiff, UK.
出版信息
J Hepatol. 1998;28 Suppl 1:26-7. doi: 10.1016/s0168-8278(98)80372-3.
PMID:9575446
Abstract
The discovery of the gene responsible for most cases of genetic haemochromatosis has made it possible to re-evaluate the role of haemochromatosis in causing iron accumulation in porphyria cutanea tarda and various inherited anaemias. Recent studies of these associations are reviewed.
摘要
导致大多数遗传性血色素沉着症病例的基因的发现，使得重新评估血色素沉着症在迟发性皮肤卟啉症和各种遗传性贫血中铁蓄积过程中的作用成为可能。本文综述了近期关于这些关联的研究。
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