A family with the Coffin Lowry syndrome revisited: localization of CLS to Xp21-pter

Am J Med Genet. 1988 May-Jun;30(1-2):509-21. doi: 10.1002/ajmg.1320300153.

Abstract

We revisited a family with the Coffin-Lowry syndrome (CLS) first reported by Procopis and Turner in 1972. Twelve affected members are now known in 3 generations of which 9 were seen personally. DNA marker studies supported X-linkage with localization of CLS to Xp near DXS43 at p22.2-22.1 (theta = 0.001 Z = 2.71). Such linkage is reinforced by positive lod scores for DXS28 (theta = 0.00, Z = 0.90) and for DXS84 (theta = 0.09, Z = 1.56). Recombination with DXS84 and DXS164 places CLS distal to DMD in Xp21-pter.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Bone Diseases, Developmental / genetics*
  • Child
  • Child, Preschool
  • Chromosome Mapping
  • Female
  • Genetic Linkage*
  • Genetic Markers
  • Humans
  • Intellectual Disability / genetics*
  • Male
  • Middle Aged
  • Pedigree
  • Syndrome
  • X Chromosome*

Substances

  • Genetic Markers