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A new locus for autosomal recessive non-syndromic mental retardation maps to 1p21.1-p13.3.

Authors :
Uyguner O
Kayserili H
Li Y
Karaman B
Nürnberg G
Hennies H
Becker C
Nürnberg P
Başaran S
Apak MY
Wollnik B
Source :
Clinical genetics [Clin Genet] 2007 Mar; Vol. 71 (3), pp. 212-9.
Publication Year :
2007

Abstract

Autosomal recessive inheritance of non-syndromic mental retardation (ARNSMR) may account for approximately 25% of all patients with non-specific mental retardation (NSMR). Although many X-linked genes have been identified as a cause of NSMR, only three autosomal genes are known to cause ARNSMR. We present here a large consanguineous Turkish family with four mentally retarded individuals from different branches of the family. Clinical tests showed cognitive impairment but no neurological, skeletal, and biochemical involvements. Genome-wide mapping using Human Mapping 10K Array showed a single positive locus with a parametric LOD score of 4.92 in a region on chromosome 1p21.1-p13.3. Further analyses using polymorphic microsatellite markers defined a 6.6-Mb critical region containing approximately 130 known genes. This locus is the fourth one linked to ARNSMR.

Details

Language :
English
ISSN :
0009-9163
Volume :
71
Issue :
3
Database :
MEDLINE
Journal :
Clinical genetics
Publication Type :
Academic Journal
Accession number :
17309643
Full Text :
https://doi.org/10.1111/j.1399-0004.2007.00762.x