Variable onset of metachromatic leukodystrophy in a Vietnamese family

被引:21
作者
Arbour, LT
Silver, K
Hechtman, P
Treacy, EP
Coulter-Mackie, MB
机构
[1] Univ British Columbia, Dept Pediat, Vancouver, BC V6H 3N1, Canada
[2] McGill Univ, Dept Human Genet, Montreal, PQ, Canada
[3] McGill Univ, Dept Pediat, Montreal, PQ H3A 2T5, Canada
[4] McGill Univ, Dept Neurol, Montreal, PQ H3A 2T5, Canada
[5] McGill Univ, Dept Biol, Montreal, PQ H3A 2T5, Canada
关键词
D O I
10.1016/S0887-8994(00)00164-8
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
We report two siblings with metachromatic leukodystrophy, one who presented at 7 years of age (juvenile onset) and his sister who presented at 22 years of age (adult onset), They are compound heterozygotes for two novel mutations in the arylsufatase ii gene (ARSA), The responsible mutations in this Vietnamese family consist of a missense mutation with 5 % enzyme activity (R143G) and a nonsense mutation (W318ter), from which no enzyme activity would be expected, These mutations in the ARSA gene have not been previously reported and may be useful when diagnosing metachromatic leukodystrophy in other affected Vietnamese individuals. The variability in presentation suggests that the genotype alone is not sufficient to determine the onset and course of the disease and modifying genetic and perhaps nongenetic factors likely contribute, (C) 2000 by Elsevier Science Inc. All rights reserved.
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页码:173 / 176
页数:4
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