雷特综合征
MECP2
错义突变
医学
突变
儿科
基因
遗传学
生物
表型
作者
K Deutscher,J. Deutscher,Linda C. Bergmann,Katrin Tefs,Kathrin Reichwald,Volker Schuster
出处
期刊:Klinische Padiatrie
[Thieme Medical Publishers (Germany)]
日期:2002-09-17
卷期号:214 (05): 291-294
摘要
We report on four mental retarded girls with typical clinical signs of Rett syndrome. Rett syndrome is an X-linked neurodevelopment disorder which develops after a period of normal development at the age of 6 to 18 months, affecting 1/10 000 - 15 000 girls. Recently, the MeCP2-gene encoding the methyl-CpG-binding protein 2 has been shown to be mutated in 80 percent of girls with Rett Syndrome, studied so far. In our patients with Rett syndrome two common mutations of the MeCP2-gene, R168X (n=2) and T158M were found. In the 4th patient a novel "missense" mutation R294G was identified.
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