| Literature DB >> 2301468 |
H Y Zoghbi1, D H Ledbetter, R Schultz, A K Percy, D G Glaze.
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.Entities:
Mesh:
Year: 1990 PMID: 2301468 DOI: 10.1002/ajmg.1320350131
Source DB: PubMed Journal: Am J Med Genet ISSN: 0148-7299