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[溶酶体贮积症的诊断与治疗新进展]

[Recent advances in the diagnosis and treatment of lysosomal storage diseases].

作者信息

Wu Xi-ru, Bao Xin-hua

机构信息

Department of Pediatrics, Peking University First Hospital, Beijing 100034, China.

出版信息

Beijing Da Xue Xue Bao Yi Xue Ban. 2005 Aug 18;37(4):440-4.

Abstract

Lysosomal storage diseases are a group of genetic disorders that result from the defect in lysosomal function. Signs and symptoms are variable, it is difficult to diagnose this group of disease merely by the clinical manifestation. The diagnosis usually is made by measuring the activity of the corresponding enzyme. Gene mutational analysis is useful for the diagnosis of some of the lysosome storage diseases. The treatment has focused on the replacement of the defective enzyme responsible for the disease and the hematopoietic stem cell transplantation. Both of them have achieved exciting outcomes in some of the diseases.

摘要

溶酶体贮积症是一组由于溶酶体功能缺陷导致的遗传性疾病。其体征和症状各不相同,仅通过临床表现很难诊断这类疾病。诊断通常通过测量相应酶的活性来进行。基因突变分析对某些溶酶体贮积症的诊断有帮助。治疗主要集中在替代导致该疾病的缺陷酶以及进行造血干细胞移植。这两种方法在某些疾病中都取得了令人振奋的成果。

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