Literature DB >> 1132165

A possible major contribution to mental retardation in the general population by the gene for microcephaly.

Q H Qazi, T E Reed.   

Abstract

In a study of 13 families with genetic microcephaly, it was found that 11 of 24 parents (two fathers not ascertained) and 11 of 33 non-microcephalic siblings were of subnormal intelligence. In a rare autosomal recessive condition, all parents and two-thirds of unaffected siblings are presumed carriers of the gene. It so, nearly 50% of all presumed heterozygotes in the present study were mentally retarded. The proportion agrees well with the other major study of microcephaly in North America, but differs from the Dutch study. On the basis of pooled data from the three studies and the estimated incidence of 1:40000 for genetic microcephaly, it is postulated that (1) about 0.34% of the general population is mentally retarded because it is carrying the gene for microcephaly and (2) about one of nine mentally retarded individuals is heterozygous for the gene for microcephaly.

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Year:  1975        PMID: 1132165     DOI: 10.1111/j.1399-0004.1975.tb00302.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


  7 in total

Review 1.  Research strategies in human behaviour genetics.

Authors:  F Vogel
Journal:  J Med Genet       Date:  1987-03       Impact factor: 6.318

Review 2.  Autosomal recessive primary microcephaly (MCPH): a review of clinical, molecular, and evolutionary findings.

Authors:  C Geoffrey Woods; Jacquelyn Bond; Wolfgang Enard
Journal:  Am J Hum Genet       Date:  2005-03-31       Impact factor: 11.025

3.  Protein-truncating mutations in ASPM cause variable reduction in brain size.

Authors:  Jacquelyn Bond; Sheila Scott; Daniel J Hampshire; Kelly Springell; Peter Corry; Marc J Abramowicz; Ganesh H Mochida; Raoul C M Hennekam; Eamonn R Maher; Jean-Pierre Fryns; Abdulrahman Alswaid; Hussain Jafri; Yasmin Rashid; Ammar Mubaidin; Christopher A Walsh; Emma Roberts; C Geoffrey Woods
Journal:  Am J Hum Genet       Date:  2003-10-21       Impact factor: 11.025

4.  Is a gene for microcephaly located on chromosome 1?

Authors:  A Pérez-Castillo; M A Martín-Lucas; J A Abrisqueta
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

5.  Autosomal recessive primary microcephaly: an analysis of locus heterogeneity and phenotypic variation.

Authors:  E Roberts; D J Hampshire; L Pattison; K Springell; H Jafri; P Corry; J Mannon; Y Rashid; Y Crow; J Bond; C G Woods
Journal:  J Med Genet       Date:  2002-10       Impact factor: 6.318

6.  Congenital malformations and developmental disabilities in ataxia-telangiectasia, Fanconi anemia, and xeroderma pigmentosum families.

Authors:  K Welshimer; M Swift
Journal:  Am J Hum Genet       Date:  1982-09       Impact factor: 11.025

7.  A fifth locus for primary autosomal recessive microcephaly maps to chromosome 1q31.

Authors:  L Pattison; Y J Crow; V J Deeble; A P Jackson; H Jafri; Y Rashid; E Roberts; C G Woods
Journal:  Am J Hum Genet       Date:  2000-11-07       Impact factor: 11.043

  7 in total

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