Literature DB >> 7188916

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

J F McLaughlin, E Kriegsmann.   

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.

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Year:  1980        PMID: 7188916     DOI: 10.1111/j.1469-8749.1980.tb04308.x

Source DB:  PubMed          Journal:  Dev Med Child Neurol        ISSN: 0012-1622            Impact factor:   5.449


  8 in total

1.  Renpenning syndrome maps to Xp11.

Authors:  R E Stevenson; J F Arena; E Ouzts; A Gibson; M H Shokeir; C Vnencak-Jones; H A Lubs; M May; C E Schwartz
Journal:  Am J Hum Genet       Date:  1998-05       Impact factor: 11.025

Review 2.  Nonspecific X-linked mental retardation--a review.

Authors:  G Tariverdian; B Weck
Journal:  Hum Genet       Date:  1982       Impact factor: 4.132

3.  Infantile autism associated with the fragile-X syndrome.

Authors:  D L Meryash; L S Szymanski; P S Gerald
Journal:  J Autism Dev Disord       Date:  1982-09

4.  The 'fragile' X chromosome in the Martin-Bell-Renpenning syndrome and in males with other forms of familial mental retardation.

Authors:  R Proops; T Webb
Journal:  J Med Genet       Date:  1981-10       Impact factor: 6.318

5.  Further delineation of X-linked mental retardation.

Authors:  D S Herbst; H G Dunn; F J Dill; D K Kalousek; L W Krywaniuk
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

6.  Novel truncating mutations in the polyglutamine tract binding protein 1 gene (PQBP1) cause Renpenning syndrome and X-linked mental retardation in another family with microcephaly.

Authors:  Claus Lenski; Fatima Abidi; Alfons Meindl; Alice Gibson; Matthias Platzer; R Frank Kooy; Herbert A Lubs; Roger E Stevenson; Juliane Ramser; Charles E Schwartz
Journal:  Am J Hum Genet       Date:  2004-04       Impact factor: 11.025

7.  Developmental Foreign Accent Syndrome: Report of a New Case.

Authors:  Stefanie Keulen; Peter Mariën; Peggy Wackenier; Roel Jonkers; Roelien Bastiaanse; Jo Verhoeven
Journal:  Front Hum Neurosci       Date:  2016-03-10       Impact factor: 3.169

8.  Cognitive, Linguistic, and Motor Abilities in a Multigenerational Family with Childhood Apraxia of Speech.

Authors:  Bronwyn Carrigg; Louise Parry; Elise Baker; Lawrence D Shriberg; Kirrie J Ballard
Journal:  Arch Clin Neuropsychol       Date:  2016-12-01       Impact factor: 2.813

  8 in total

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