Nonsyndromic X-linked mental retardation: mapping of MRX58 to the pericentromeric region

Am J Med Genet. 1999 Sep 10;86(2):102-6. doi: 10.1002/(sici)1096-8628(19990910)86:2<102::aid-ajmg2>3.0.co;2-c.

Abstract

An Austrian family with nonsyndromic X-linked mental retardation (MRX) is reported in which the obligatory carrier females are normal, and 5 affected males have mild to moderate mental retardation. Linkage analysis indicated an X pericentromeric localization, with flanking markers DXS989 and DXS1111 and a maximum multipoint LOD score of 2.09 (straight theta = 0) for the 7 cosegregating markers DXS1243, CybB, MAOB, DXS988, ALAS2, DXS991, and AR. MRX58 thus mapped within a 50-cM interval between Xp11.3 and Xq13.1 and overlapped with 23 other MRX families already described. This pericentromeric clustering of MRX families suggests allelism, with a minimum of 2 X-linked mental retardation (XLMR) genes in this region.

MeSH terms

  • Centromere / genetics
  • Chromosome Mapping
  • Cytogenetics
  • Family Health
  • Female
  • Genetic Linkage
  • Humans
  • Intellectual Disability / genetics*
  • Lod Score
  • Male
  • Microsatellite Repeats
  • Pedigree
  • X Chromosome / genetics*