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PMID: 7188916 Published · ppublish English Case Reports Journal Article Research Support, U.S. Gov't, Non-P.H.S.

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

Developmental medicine and child neurology ·Vol. 22 ·No. 1 ·1980-02-00 ·Pages 84-92

McLaughlin JF, Kriegsmann E

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.

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
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
McLaughlin J F
Kriegsmann E
Article Info
Journal
Developmental medicine and child neurology
Abbr.
Dev Med Child Neurol
ISSN
0012-1622
Published
1980-02-00
Pages
84-92
Language
English
Region
England
NLM ID
0006761
Subset
IM
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