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土耳其芳基硫酸酯酶A假缺陷的发生率。

Arylsulfatase A pseudodeficiency incidence in Turkey.

作者信息

Emre S, Topçu M, Terzioğlu M, Renda Y

机构信息

Department of Medical Biology, Hacettepe University Faculty of Medicine, Ankara, Turkey.

出版信息

Turk J Pediatr. 2000 Apr-Jun;42(2):115-7.

Abstract

Pseudodeficiency (Pd) in arylsulfatase A (ASA) is a relatively frequent condition in healthy individuals. It produces a reduction in enzyme activity similar to that found in metachromatic leukodystrophy (MLD). A variable incidence of the Pd allele was found in different populations; it was 10-20 times higher than that of metachromatic leukodystrophy. Twelve of the 52 unrelated, healthy individuals were found to be heterozygous for the ASA Pd allele. In Turkey we estimated the incidence of the Pd allele as 11.5 percent. Out of 18 cases with MLD, one patient was found homozygous for the Pd allele and the other patient was found heterozygous.

摘要

芳基硫酸酯酶A(ASA)的假缺陷(Pd)在健康个体中是一种相对常见的情况。它会导致酶活性降低,类似于在异染性脑白质营养不良(MLD)中发现的情况。在不同人群中发现Pd等位基因的发生率各不相同;它比异染性脑白质营养不良的发生率高10至20倍。在52名无亲缘关系的健康个体中,有12人被发现为ASA Pd等位基因的杂合子。在土耳其,我们估计Pd等位基因的发生率为11.5%。在18例MLD患者中,有1例患者被发现为Pd等位基因的纯合子,另1例患者为杂合子。

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