Linkage mapping of a new syndromic form of X-linked mental retardation, MRXS7, associated with obesity

Eur J Hum Genet. 1999 Oct-Nov;7(7):828-32. doi: 10.1038/sj.ejhg.5200376.

Abstract

A new syndromic form of X-linked mental retardation associated to obesity, MRXS7, has been localised to Xp11.3-Xq23 in a large Pakistani family. The ten affected males show clinical manifestations of mental retardation, obesity and hypogonadism. The family was genotyped by a set of microsatellite markers spaced at approximately 10 cM intervals on the X chromosome. Linkage to five adjacent microsatellite markers, mapping in the pericentromeric area, was established and a maximum two-point lod score of 3.86 was reached at zero recombination with marker DXS1106. Reduced recombination events around the centromere prevented precise mapping of the gene.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Chromosome Mapping*
  • Female
  • Genetic Linkage / genetics*
  • Humans
  • Intellectual Disability / genetics*
  • Lod Score
  • Male
  • Middle Aged
  • Obesity / genetics*
  • Pedigree
  • Syndrome
  • X Chromosome / genetics*