The Coffin-Lowry syndrome. A study of two new index patients and their families

Eur J Pediatr. 1984 Dec;143(2):82-6. doi: 10.1007/BF00445790.

Abstract

Two adult, mentally retarded males with the typical features of the Coffin-Lowry syndrome are reported. Further family investigation led to the same diagnosis in a 2.5-year-old male cousin, and to the identification of five female carriers, with variable clinical expression of this X-linked inherited mental retardation syndrome.

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Bone Diseases, Developmental / genetics*
  • Child
  • Child, Preschool
  • Facial Expression
  • Female
  • Fingers / abnormalities
  • Genetic Linkage
  • Heterozygote
  • Humans
  • Intellectual Disability / genetics*
  • Male
  • Middle Aged
  • Pedigree
  • X Chromosome