Literature DB >> 6931286

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

G Turner, R Brookwell, A Daniel, M Selikowitz, M Zilibowitz.   

Abstract

Males affected by one form of X-linked retardation possess the X-chromosomal marker fra(X)(q27) and are physically normal except for macro-orchidism. To relate possession of the marker X to phenotypic expression in female heterozygotes, we investigated 128 mildly retarded (IQ, 55 to 75) school-girls in Sydney, New South Wales, Australia. Seventy-two girls had no physical abnormalities and of these, five (7 per cent) carried the marker X. Investigation of relatives revealed retarded males in four of the five families. Pedigree and chromosomal analysis identified a further 18 heterozygotes; six were regarded as intellectually or educationally retarded. We conclude that expression of the X-linked mutation in female carriers contributes to mild mental retardation of girls, that those who are physically normal should be screened for the marker X, and that their relatives should be investigated in order to identify additional females with a high risk of conceiving affected males.

Entities:  

Mesh:

Substances:

Year:  1980        PMID: 6931286     DOI: 10.1056/NEJM198009183031202

Source DB:  PubMed          Journal:  N Engl J Med        ISSN: 0028-4793            Impact factor:   91.245


  58 in total

1.  Fragile X syndrome among children with mental retardation.

Authors:  R Elango; I C Verma
Journal:  Indian J Pediatr       Date:  1996 Jul-Aug       Impact factor: 1.967

2.  Neuropsychological deficits in obligatory heterozygotes for metachromatic leukodystrophy.

Authors:  H Kohn; P Manowitz; M Miller; A Kling
Journal:  Hum Genet       Date:  1988-05       Impact factor: 4.132

3.  Selection in blood cells from female carriers of the fragile X syndrome: inverse correlation between age and proportion of active X chromosomes carrying the full mutation.

Authors:  F Rousseau; D Heitz; I Oberlé; J L Mandel
Journal:  J Med Genet       Date:  1991-12       Impact factor: 6.318

4.  A community study of severe mental retardation in the West Midlands and the importance of the fragile X chromosome in its aetiology.

Authors:  S Bundey; T P Webb; A Thake; J Todd
Journal:  J Med Genet       Date:  1985-08       Impact factor: 6.318

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.  Clinical and cytogenetic survey of institutionalized mentally retarded patients with emphasis on the fragile-X syndrome.

Authors:  M G Butler; D N Singh
Journal:  J Intellect Disabil Res       Date:  1993-04

Review 7.  The fragile X syndrome: the patients and their chromosomes.

Authors:  M A De Arce; A Kearns
Journal:  J Med Genet       Date:  1984-04       Impact factor: 6.318

8.  Frequency of the fragile X syndrome in institutionalized mentally retarded females in Japan.

Authors:  T Arinami; I Kondo; S Nakajima; H Hamaguchi
Journal:  Hum Genet       Date:  1987-08       Impact factor: 4.132

9.  Cognitive, behavioral, and adaptive functioning in fragile X and non-fragile X retarded men.

Authors:  E Dykens; J Leckman; R Paul; M Watson
Journal:  J Autism Dev Disord       Date:  1988-03

10.  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

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.