对患雷特综合征的同卵双胞胎进行随访。
Follow-up of monozygotic twins concordant for the Rett syndrome.
作者信息
Tariverdian G
机构信息
Institute for Humangenetics and Anthropology, Heidelberg University, Federal Republic of Germany.
出版信息
Brain Dev. 1990;12(1):125-7. doi: 10.1016/s0387-7604(12)80192-6.
PMID:2344007
Abstract
The clinical features and follow-up of monozygotic twins with the Rett syndrome (RS) are described. The twins are almost concordant in all clinical signs. This identity indicates a genetic cause of RS. A clinical follow-up confirmed the diagnosis.
摘要
本文描述了患有雷特综合征（RS）的单卵双胞胎的临床特征及随访情况。这对双胞胎在所有临床体征上几乎完全一致。这种一致性表明雷特综合征存在遗传病因。临床随访证实了该诊断。
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