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黏多糖贮积症:生物化学与临床症状

The mucopolysaccharidoses: biochemistry and clinical symptoms.

作者信息

Kresse H, Cantz M, von Figura K, Glössl J, Paschke E

出版信息

Klin Wochenschr. 1981 Aug 17;59(16):867-76. doi: 10.1007/BF01721920.

Abstract

The mucopolysaccharidoses are a group of genetic diseases which are characterized by an excessive intralysosomal accumulation of partially degraded mucopolysaccharides. This storage is caused by the inactivity of one of eleven enzymes that are required for the degradation of the different types of mucopolysaccharides. There is a rough correlation between phenotype and chemical nature of the storage material. Similar clinical pictures, however, may be caused by an inactivity of different enzymes. Conversely, different clinical expressions of the defect of a single enzyme may be attributed to allelic mutations. The recent development of specific assay procedures for the respective enzymes allows 1. an early genotype-specific diagnosis of affected patients, 2. prenatal diagnosis of the metabolic defect in families at risk, 3. to prognosticate the course of the disease at least in some instances, and 4. genetic counseling for members of affected families. At present, there is no specific therapy. Attempts of enzyme replacement therapy are still at an experimental stage.

摘要

黏多糖贮积症是一组遗传性疾病,其特征是溶酶体内部分降解的黏多糖过度蓄积。这种蓄积是由于降解不同类型黏多糖所需的11种酶之一缺乏活性所致。贮积物质的表型与化学性质之间存在大致的相关性。然而,不同酶的缺乏活性可能导致相似的临床表现。相反,单一酶缺陷的不同临床表型可能归因于等位基因突变。针对相应酶的特异性检测方法的最新进展使得:1. 能够对受影响患者进行早期基因型特异性诊断;2. 对有风险家庭中的代谢缺陷进行产前诊断;3. 至少在某些情况下预测疾病进程;4. 为受影响家庭的成员提供遗传咨询。目前,尚无特异性治疗方法。酶替代疗法仍处于实验阶段。

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