[由 HAMP 基因突变引起的轻度遗传性血色病病例报告]。

Q3 Medicine
Z Wang, W Hou, H Zheng
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引用次数: 0

摘要

HAMP基因突变导致的幼年遗传性血色病发病率较低,在中国鲜有报道。该患者以肝功能异常为首发症状,最终通过基因检测和肝组织病理学检查确诊,并进行了静脉放血治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[A case report of mild hereditary hemochromatosis caused by HAMP gene mutation].

The incidence of juvenile Hereditary Hemochromatosis caused by HAMP gene mutation is low, which is rarely reported in China. This patient took abnormal liver function as the first symptom, and was finally diagnosed by genetic testing and hepatic histopathology, and treated by venous bloodletting.

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来源期刊
中华肝脏病杂志
中华肝脏病杂志 Medicine-Medicine (all)
CiteScore
1.20
自引率
0.00%
发文量
7574
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