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A de novo X;3 translocation in Rett syndrome.

作者信息

Zoghbi H Y, Ledbetter D H, Schultz R, Percy A K, Glaze D G

机构信息

Department of Pediatrics, Baylor College of Medicine, Houston, Texas 77030.

出版信息

Am J Med Genet. 1990 Jan;35(1):148-51. doi: 10.1002/ajmg.1320350131.

Abstract

Rett syndrome is a neurodegenerative disorder that occurs exclusively in females. The syndrome is sporadic in most cases with the exception of a few familial cases with an inheritance pattern through maternal lines. These observations raised the possibility that Rett syndrome may be due to an X-linked dominant mutation which is lethal in the male. To evaluate this hypothesis, we have systematically performed high-resolution chromosome analysis on 28 patients with Rett syndrome searching for deletions and/or translocations. In one patient, a de novo balanced translocation was observed with the chromosome constitution of 46,X,t(X;3) (p22.11;q13.31). This finding supports the hypothesis of an X-linked dominant mutation and suggests that the Rett gene might map to distal Xp21 or proximal Xp22.

摘要

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