Suppr超能文献

由于葡萄糖-6-磷酸转运酶缺陷导致的1b型糖原贮积病。

Glycogen storage disease type 1b due to a defect of glucose-6-phosphate translocase.

作者信息

Narisawa K, Otomo H, Igarashi Y, Arai N, Otake M, Tada K, Kuzuya T

出版信息

J Inherit Metab Dis. 1982;5(4):227-8. doi: 10.1007/BF02179148.

Abstract

Patients with glycogen storage disease (GSD) type 1b have shown normal activity of glucose-6-phosphatase (EC 3.1.3.9) as assayed in frozen liver, though their clinical and biochemical findings were similar to those of patients with GSD 1a (McKusick 23220) (Senior and Loridan, 1968). In 1978, we suggested that a basic defect of GSD 1b exists in the glucose-6-phosphate (G6P) transport system (Narisawa et al., 1978; Igarashi et al., 1979). Since then, there have been reports confirming our observation (Beaudet et al., 1980; Lange et al., 1980; Corbeel et al., 1981; Schaub et al., 1981). Recently, it was postulated that the G6Pase system contains a phosphate translocase which mediates the efflux of phosphate, in addition to a G6P translocase and a non-specific phosphohydrolase (Arion et al., 1980). Therefore, it is possible that GSD 1b is caused by a defect of phosphate translocase. In this paper, the basic defect in GSD type 1b was investigated in two patients; one with severe, the other with mild, clinical symptoms.

摘要

1b型糖原贮积病(GSD)患者的冰冻肝脏中葡萄糖-6-磷酸酶(EC 3.1.3.9)活性检测显示正常,尽管其临床和生化表现与1a型GSD患者相似(麦库西克23220)(西尼尔和洛里丹,1968年)。1978年,我们提出1b型GSD的基本缺陷存在于葡萄糖-6-磷酸(G6P)转运系统中(成泽等人,1978年;五十岚等人,1979年)。从那时起,已有报告证实了我们的观察结果(博德特等人,1980年;兰格等人,1980年;科比尔等人,1981年;绍布等人,1981年)。最近有人提出,G6P酶系统除了含有G6P转运体和非特异性磷酸水解酶外,还含有一种介导磷酸盐外流的磷酸盐转运体(阿里昂等人,1980年)。因此,1b型GSD有可能是由磷酸盐转运体缺陷引起的。在本文中,对两名患者进行了1b型GSD基本缺陷的研究;一名有严重临床症状,另一名有轻度临床症状。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验