Literature DB >> 2333902

Another model for the inheritance of Rett syndrome.

E M Bühler1, N J Malik, M Alkan.   

Abstract

The fact that probably less than 1% of Rett syndrome cases are familial speaks in favor of a spontaneous mutation as the most common cause of Rett syndrome. However, the few familial cases (about 10) described in the literature, the elevated consanguinity rate in parents of Rett patients (2.4% vs. 0.5%), and the existence of "formes frustes" in relatives of Rett girls, suggest that inheritance must exist. A model based on a hypothetical form of inheritance, namely allelic and non-allelic metabolic interference, fits almost all available data, as well as the exclusive occurrence in females without increased abortion rate.

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Year:  1990        PMID: 2333902     DOI: 10.1002/ajmg.1320360125

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


  9 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.  A new Rett syndrome family consistent with X-linked inheritance expands the X chromosome exclusion map.

Authors:  N C Schanen; E J Dahle; F Capozzoli; V A Holm; H Y Zoghbi; U Francke
Journal:  Am J Hum Genet       Date:  1997-09       Impact factor: 11.025

3.  Rett syndrome, classical and atypical: genealogical support for common origin.

Authors:  H O Akesson; B Hagberg; J Wahlström
Journal:  J Med Genet       Date:  1996-09       Impact factor: 6.318

Review 4.  Rett syndrome.

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

5.  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

6.  Mutation screening in Rett syndrome patients.

Authors:  F Xiang; S Buervenich; P Nicolao; M E Bailey; Z Zhang; M Anvret
Journal:  J Med Genet       Date:  2000-04       Impact factor: 6.318

7.  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

8.  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

9.  Studies of X inactivation and isodisomy in twins provide further evidence that the X chromosome is not involved in Rett syndrome.

Authors:  B R Migeon; M A Dunn; G Thomas; B J Schmeckpeper; S Naidu
Journal:  Am J Hum Genet       Date:  1995-03       Impact factor: 11.025

  9 in total

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