Literature DB >> 2301468

A de novo X;3 translocation in Rett syndrome.

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.

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Year:  1990        PMID: 2301468     DOI: 10.1002/ajmg.1320350131

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  13 in total

1.  Some remarks regarding the search for a genetic basis for Rett syndrome.

Authors:  E M Bühler
Journal:  Hum Genet       Date:  1991-06       Impact factor: 4.132

2.  Rett syndrome: exclusion mapping following the hypothesis of germinal mosaicism for new X-linked mutations.

Authors:  N Archidiacono; M Lerone; M Rocchi; M Anvret; T Ozcelik; U Francke; G Romeo
Journal:  Hum Genet       Date:  1991-04       Impact factor: 4.132

3.  Examination of X chromosome markers in Rett syndrome: exclusion mapping with a novel variation on multilocus linkage analysis.

Authors:  K A Ellison; C P Fill; J Terwilliger; L J DeGennaro; A Martin-Gallardo; M Anvret; A K Percy; J Ott; H Zoghbi
Journal:  Am J Hum Genet       Date:  1992-02       Impact factor: 11.025

4.  Linkage analysis in Rett syndrome families suggests that there may be a critical region at Xq28.

Authors:  T Webb; A Clarke; F Hanefeld; J L Pereira; L Rosenbloom; C G Woods
Journal:  J Med Genet       Date:  1998-12       Impact factor: 6.318

Review 5.  Rett syndrome.

Authors:  A Clarke
Journal:  J Med Genet       Date:  1996-08       Impact factor: 6.318

6.  Chromosome mapping of Rett syndrome: a likely candidate region on the telomere of Xq.

Authors:  F Xiang; Z Zhang; A Clarke; P Joseluiz; N Sakkubai; B Sarojini; C D Delozier-Blanchet; I Hansmann; L Edström; M Anvret
Journal:  J Med Genet       Date:  1998-04       Impact factor: 6.318

Review 7.  Rett syndrome.

Authors:  S B Naidu
Journal:  Indian J Pediatr       Date:  1997 Sep-Oct       Impact factor: 1.967

Review 8.  Mendelian cytogenetics. Chromosome rearrangements associated with mendelian disorders.

Authors:  N Tommerup
Journal:  J Med Genet       Date:  1993-09       Impact factor: 6.318

9.  X chromosome inactivation in 30 girls with Rett syndrome: analysis using the probe.

Authors:  P Camus; N Abbadi; M C Perrier; M Chéry; S Gilgenkrantz
Journal:  Hum Genet       Date:  1996-02       Impact factor: 4.132

10.  X chromosome linkage studies in familial Rett syndrome.

Authors:  A R Curtis; S Headland; S Lindsay; N S Thomas; E Boye; S Kamakari; P Roustan; M Anvret; J Wahlstrom; G McCarthy
Journal:  Hum Genet       Date:  1993-01       Impact factor: 4.132

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