Literature DB >> 2421647

Chromosome abnormalities in pupils attending ESN/M schools.

M A Lamont, N R Dennis, M Seabright.   

Abstract

One hundred and sixty six children attending educationally subnormal/mild (ESN/M) schools were karyotyped as part of a project investigating the aetiology of mild mental retardation. Nine had significant chromosome abnormalities. Five of six children identified during the survey had no dysmorphic features--47,XXY (two), 48,XXYY, 46,XX 15q-, and 46,XX,t(X;19). One dysmorphic boy had a balanced translocation--46,XY,t(3;15). Three were already known--47,XX+21 (two) and 46,XY, 14q+. We suggest that routine karyotyping of children with mild mental retardation be considered.

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Year:  1986        PMID: 2421647      PMCID: PMC1777694          DOI: 10.1136/adc.61.3.223

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


  17 in total

1.  Clinical assessment of 4500 developmentally delayed individuals.

Authors:  S L Einfeld
Journal:  J Ment Defic Res       Date:  1984-06

2.  Mild mental retardation in Swedish school children. II. Etiologic and pathogenetic aspects.

Authors:  B Hagberg; G Hagberg; A Lewerth; U Lindberg
Journal:  Acta Paediatr Scand       Date:  1981-07

3.  Fragile site X chromosomes and X-linked mental retardation in severely retarded boys in a northern Swedish county. A prevalence study.

Authors:  H K Blomquist; K H Gustavson; G Holmgren; I Nordenson; A Sweins
Journal:  Clin Genet       Date:  1982-03       Impact factor: 4.438

4.  Marker X-associated mental retardation. A study of 150 retarded males.

Authors:  M Kähkönen; J Leisti; M Wilska; S Varonen
Journal:  Clin Genet       Date:  1983-06       Impact factor: 4.438

5.  Klinefelter's syndrome in adolescence.

Authors:  S G Ratcliffe; J Bancroft; D Axworthy; W McLaren
Journal:  Arch Dis Child       Date:  1982-01       Impact factor: 3.791

6.  Prader-Willi syndrome and chromosome 15. A clinical discussion of 20 cases.

Authors:  J F Mattei; M G Mattei; F Giraud
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132

7.  Fragile X syndrome in mildly mentally retarded children in a northern Swedish county. A prevalence study.

Authors:  H K Blomquist; K H Gustavson; G Holmgren; I Nordenson; U Pålsson-Stråe
Journal:  Clin Genet       Date:  1983-12       Impact factor: 4.438

8.  Deletions of proximal 15q and non-classical Prader-Willi syndrome phenotypes.

Authors:  S Schwartz; S R Max; S R Panny; M M Cohen
Journal:  Am J Med Genet       Date:  1985-02

9.  Heterozygous expression of X-linked mental retardation and X-chromosome marker fra(X)(q27).

Authors:  G Turner; R Brookwell; A Daniel; M Selikowitz; M Zilibowitz
Journal:  N Engl J Med       Date:  1980-09-18       Impact factor: 91.245

10.  Detection of the fragile X chromosome and other fragile sites.

Authors:  F Hecht; G R Sutherland
Journal:  Clin Genet       Date:  1984-10       Impact factor: 4.438

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  4 in total

1.  Diagnostic classification of the aetiology of mental retardation in children.

Authors:  M A Lamont; N R Dennis
Journal:  Br Med J (Clin Res Ed)       Date:  1987-03-21

2.  Survey of adolescents with severe intellectual handicap.

Authors:  J C Asthana; S Sinha; J S Haslam; H M Kingston
Journal:  Arch Dis Child       Date:  1990-10       Impact factor: 3.791

3.  Aetiology of mild mental retardation.

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

4.  Attitudes of the mildly mentally retarded children's parents toward their children's handicap: Dammam - Saudi Arabia.

Authors:  K Ai-Dawood; A Albar
Journal:  J Family Community Med       Date:  1994-01
  4 in total

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