Literature DB >> 7726237

Paracentric inversion X(q21.2q24) associated with mental retardation in males and normal ovarian function in females.

D Abeliovich1, J Dagan, C Kimchi-Sarfaty, J Zlotogora.   

Abstract

We describe a familial paracentric inversion (X)(q21.2 q24) in a family with 2 male and 2 female carriers. The males were mentally retarded and the females were normal with normal ovarian function. It is suggested that a recessive mental retardation (MR) gene was disrupted by one of the inversion breakpoints, although an X-linked MR gene which by chance is linked to the inv(X) could not be ruled out. In the female carriers of the paracentric inversion a random X-inactivation was demonstrated. The normal ovarian function is an exception to the concept of "critical region" at Xq13-q26.

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Year:  1995        PMID: 7726237     DOI: 10.1002/ajmg.1320550322

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


  3 in total

1.  Localisation of two candidate genes for mental retardation using a YAC physical map of the Xq21.1-21.2 subbands.

Authors:  L Colleaux; M May; J Belougne; D Lepaslier; C Schwartz; M Fontes
Journal:  J Med Genet       Date:  1996-05       Impact factor: 6.318

2.  Characterisation of an inverted X chromosome (p11.2q21.3) associated with mental retardation using FISH.

Authors:  F Sloan-Béna; C Philippe; B LeHeup; F Wuilque; E R Levy; M Chéry; P Jonveaux; A P Monaco
Journal:  J Med Genet       Date:  1998-02       Impact factor: 6.318

3.  Localisation of a new gene for non-specific mental retardation to Xq22-q26 (MRX35).

Authors:  X X Gu; R Decorte; P Marynen; J P Fryns; J J Cassiman; P Raeymaekers
Journal:  J Med Genet       Date:  1996-01       Impact factor: 6.318

  3 in total

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