SHOX gene mutations and deletions in dyschondrosteosis or Leri-Weill syndrome

Acta Paediatr Suppl. 1999 Dec;88(433):55-9. doi: 10.1111/j.1651-2227.1999.tb14404.x.

Abstract

Dyschondrosteosis is an autosomal dominant form of mesomelic dysplasia that is often combined with a deformity of the forearms called Madelung deformity. Based on the observation of X-Y translocations (p22,q12) in patients with dyschondrosteosis, the authors tested the pseudoautosomal region in eight affected families and showed linkage of the dyschondrosteosis gene to a microsatellite DNA marker at the DXYS233 locus (Zmax = 6.26 at theta = 0). Since the short stature homeobox-containing gene (SHOX) involved in idiopathic growth retardation and possibly Turner syndrome maps to this region, SHOX was regarded as a strong candidate gene for dyschondrosteosis. This article reports the detection of large-scale SHOX deletions in seven of the eight families and a nonsense mutation of SHOX in the remaining family affected with dyschondrosteosis. Additional evidence suggests that Langer mesomelic dwarfism results from homozygous mutations at the genetic locus responsible for dyschondrosteosis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bone Diseases / genetics*
  • Child
  • Chromosome Deletion*
  • Dwarfism / genetics
  • Forearm / abnormalities*
  • Genetic Linkage
  • Growth Disorders / genetics*
  • Homeodomain Proteins / genetics*
  • Humans
  • Microsatellite Repeats
  • Mutation
  • Pedigree
  • Short Stature Homeobox Protein
  • Syndrome

Substances

  • Homeodomain Proteins
  • SHOX protein, human
  • Short Stature Homeobox Protein