Literature DB >> 3953670

The Martin-Bell syndrome in South Africa.

P A Venter, J Op't Hof, D J Coetzee.   

Abstract

A national screening programme was introduced in 1980 when the first cases with the Martin-Bell syndrome were diagnosed in South Africa. This survey includes patients from all the major population groups in South Africa. One thousand patients, who include 354 relatives of 21 index cases, were investigated cytogenetically. About 75% of the 354 relatives were either affected males or obligate or possible carriers. The segregation pattern of the fragile site was investigated in 271 offspring of 58 carrier women. At least 30% of the carriers were mildly mentally retarded with most expressing the fragile site. Various other investigations, such as measurements of testes, speech, verbal and IQ evaluations and hormone studies were done on several affected males. No fragile site could be demonstrated in 57 unselected autistic children. The results of this programme show that this syndrome is a common cause of mental retardation and that prevention of mental retardation is possible if all the involved families could be identified.

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Year:  1986        PMID: 3953670     DOI: 10.1002/ajmg.1320230154

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  5 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

Review 2.  Medical genetics in South Africa.

Authors:  T Jenkins
Journal:  J Med Genet       Date:  1990-12       Impact factor: 6.318

3.  Molecular evidence that fragile X syndrome occurs in the South African black population.

Authors:  A Goldman; T Jenkins; A Krause
Journal:  J Med Genet       Date:  1998-10       Impact factor: 6.318

Review 4.  Brief report: low frequency of the fragile X syndrome among Japanese autistic subjects.

Authors:  O Hashimoto; Y Shimizu; Y Kawasaki
Journal:  J Autism Dev Disord       Date:  1993-03

5.  Why are autism and the fragile-X syndrome associated? Conceptual and methodological issues.

Authors:  I L Cohen; V Sudhalter; A Pfadt; E C Jenkins; W T Brown; P M Vietze
Journal:  Am J Hum Genet       Date:  1991-02       Impact factor: 11.025

  5 in total

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