Developmental dyspraxia in a family with X-linked mental retardation (Renpenning syndrome)

Dev Med Child Neurol. 1980 Feb;22(1):84-92. doi: 10.1111/j.1469-8749.1980.tb04308.x.

Abstract

This paper describes the existence of severe developmental speech dyspraxia in a member of a family that is typical of other reports of X-linked mental retardation without physical abnormality (Renpenning syndrome). Other family members have evidence of motor or speech dyspraxia. Other reports of X-linked mental retardation have mentioned "verbal disability", which suggests that developmental dyspraxia may be quite common in these families. Developmental dyspraxia of speech is amenable to specific types of intervention: after two years of such intervention our patient's adaptive skills reflect his normal non-verbal intellectual ability, despite persistent speech deficits. This functional improvement shows how important it is to identify dyspraxia in young children, who may otherwise be labelled mentally retarded.

Publication types

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

MeSH terms

  • Apraxias / therapy
  • Child
  • Child, Preschool
  • Female
  • Follow-Up Studies
  • Humans
  • Intellectual Disability / genetics*
  • Language Development Disorders / genetics*
  • Language Disorders / genetics*
  • Male
  • Megacolon / genetics
  • Pedigree
  • X Chromosome