Literature DB >> 2248505

Survey of adolescents with severe intellectual handicap.

J C Asthana1, S Sinha, J S Haslam, H M Kingston.   

Abstract

A diagnostic survey was undertaken of children aged 11 to 19 years in Tameside with severe learning difficulties (intelligence quotient less than or equal to 50). Eighty-two children were identified and their medical records reviewed. A specific diagnosis for the retardation was documented in 25 (30%) of the children, 18 of whom had Down's syndrome. A probable aetiology or a disorder of unknown aetiology had been identified in a further 21 (26%) children. To confirm the existing diagnosis, identify new diagnoses, and offer genetic counselling, the parents of 63 children were offered detailed reassessment of their child. Fifty three children were reviewed, and a specific disorder identified in 25 out of 31 previously undiagnosed children. The most frequent diagnoses made were fragile X syndrome and Rett's syndrome. On completion of the survey, 61 of the 82 children (74%) had a specific diagnosis or probable aetiology identified, 12 (15%) had associated disorders such as cerebral palsy, and in only nine of the 82 children (11%) were there no clues at all to the cause of their retardation.

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Year:  1990        PMID: 2248505      PMCID: PMC1792345          DOI: 10.1136/adc.65.10.1133

Source DB:  PubMed          Journal:  Arch Dis Child        ISSN: 0003-9888            Impact factor:   3.791


  31 in total

1.  Rett syndrome--natural history in 70 cases.

Authors:  S Naidu; M Murphy; H W Moser; A Rett
Journal:  Am J Med Genet Suppl       Date:  1986

2.  Rett syndrome: a suggested staging system for describing impairment profile with increasing age towards adolescence.

Authors:  B Hagberg; I Witt-Engerström
Journal:  Am J Med Genet Suppl       Date:  1986

3.  Rett syndrome: studies of 13 affected girls.

Authors:  S S Budden
Journal:  Am J Med Genet Suppl       Date:  1986

Review 4.  The risk of having a second retarded child.

Authors:  H Costeff; L Weller
Journal:  Am J Med Genet       Date:  1987-08

5.  Prevalence of the fragile X syndrome in four birth cohorts of children of school age.

Authors:  M Kähkönen; T Alitalo; E Airaksinen; R Matilainen; K Launiala; S Autio; J Leisti
Journal:  Hum Genet       Date:  1987-09       Impact factor: 4.132

6.  A genetic-diagnostic survey in an institutionalized population of 173 severely mentally retarded patients.

Authors:  J P Fryns; A Kleczkowska; A Dereymaeker; M Hoefnagels; G Heremans; J Marien; H van den Berghe
Journal:  Clin Genet       Date:  1986-10       Impact factor: 4.438

7.  The frequency of the fragile X chromosome among schoolchildren in Coventry.

Authors:  T P Webb; S Bundey; A Thake; J Todd
Journal:  J Med Genet       Date:  1986-10       Impact factor: 6.318

8.  Preventive screening for the fragile X syndrome.

Authors:  G Turner; H Robinson; S Laing; S Purvis-Smith
Journal:  N Engl J Med       Date:  1986-09-04       Impact factor: 91.245

9.  Aetiology of mild mental retardation.

Authors:  M A Lamont; N R Dennis
Journal:  Arch Dis Child       Date:  1988-09       Impact factor: 3.791

10.  A cytogenetic study of mentally retarded school children in Taiwan with special reference to the fragile X chromosome.

Authors:  S Y Li; C C Tsai; M Y Chou; J K Lin
Journal:  Hum Genet       Date:  1988-08       Impact factor: 4.132

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  2 in total

1.  Isolated neurodevelopmental delay in childhood: clinicoradiological correlation in 170 patients.

Authors:  P Demaerel; D P Kingsley; B E Kendall
Journal:  Pediatr Radiol       Date:  1993

2.  D-cycloserine improves synaptic transmission in an animal model of Rett syndrome.

Authors:  Elisa S Na; Héctor De Jesús-Cortés; Arlene Martinez-Rivera; Zeeba D Kabir; Jieqi Wang; Vijayashree Ramesh; Yasemin Onder; Anjali M Rajadhyaksha; Lisa M Monteggia; Andrew A Pieper
Journal:  PLoS One       Date:  2017-08-16       Impact factor: 3.240

  2 in total

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