Coffin-Lowry syndrome: a multicenter study

Clin Genet. 1988 Oct;34(4):230-45. doi: 10.1111/j.1399-0004.1988.tb02870.x.

Abstract

The Coffin-Lowry syndrome is an inherited syndrome of mental retardation, characteristic facies and skeletal anomalies. The occurrence of severe manifestations in males, with no instance of male-to-male transmission, suggests an X-linked inheritance. The paper describes seven families from five European Centers.

Publication types

  • Case Reports
  • Clinical Trial
  • Multicenter Study

MeSH terms

  • Adult
  • Child
  • Dermatoglyphics
  • Facial Bones / abnormalities*
  • Female
  • Genetic Linkage
  • Humans
  • Intellectual Disability / genetics*
  • Karyotyping
  • Male
  • Multicenter Studies as Topic
  • Pedigree
  • Skull / abnormalities*
  • X Chromosome