Literature DB >> 8044647

A five-year prospective study of the health of children in different ethnic groups, with particular reference to the effect of inbreeding.

S Bundey1, H Alam.   

Abstract

A 5-year prospective study of 4,934 children of different ethnic groups has demonstrated a 3-fold increase of postneonatal mortality and childhood morbidity in the offspring of consanguineous Pakistani parents. Most of these families contained more than one consanguineous union, resulting in a mean inbreeding coefficient for their children of 0.0686. It is estimated that 60% of the mortality and severe morbidity of this group of children could be eliminated if inbreeding ceased. However consanguinity is much favoured in this minority group, and health education will have to be carefully and sensitively handled.

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Year:  1993        PMID: 8044647     DOI: 10.1159/000472414

Source DB:  PubMed          Journal:  Eur J Hum Genet        ISSN: 1018-4813            Impact factor:   4.246


  34 in total

1.  Consanguinity and advanced maternal age as risk factors for reproductive losses in Alexandria, Egypt.

Authors:  M M Mokhtar; M M Abdel-Fattah
Journal:  Eur J Epidemiol       Date:  2001       Impact factor: 8.082

2.  Recessive disorders and consanguineous marriage.

Authors:  John W T Benson
Journal:  BMJ       Date:  2005-12-17

3.  The representation of ethnic minorities at genetic clinics in Birmingham.

Authors:  A Roberts; R Cullen; S Bundey
Journal:  J Med Genet       Date:  1996-01       Impact factor: 6.318

4.  Translating genetics leaflets into languages other than English: lessons from an assessment of Urdu materials.

Authors:  Alison Shaw; Mushtaq Ahmed
Journal:  J Genet Couns       Date:  2004-08       Impact factor: 2.537

5.  A novel founder MYO15A frameshift duplication is the major cause of genetic hearing loss in Oman.

Authors:  Flavia Palombo; Nadia Al-Wardy; Guido Alberto Gnecchi Ruscone; Manuela Oppo; Mohammed Nasser Al Kindi; Andrea Angius; Khalsa Al Lamki; Giorgia Girotto; Tania Giangregorio; Matteo Benelli; Alberto Magi; Marco Seri; Paolo Gasparini; Francesco Cucca; Marco Sazzini; Mazin Al Khabori; Tommaso Pippucci; Giovanni Romeo
Journal:  J Hum Genet       Date:  2016-10-13       Impact factor: 3.172

6.  Congenital and genetic disorders in the Sultanate of Oman. First attempt to assess healthcare needs.

Authors:  A Rajab; Q Al Salmi; J Jaffer; A J Mohammed; M A Patton
Journal:  J Community Genet       Date:  2014-03-02

7.  Quantification of homozygosity in consanguineous individuals with autosomal recessive disease.

Authors:  C Geoffrey Woods; James Cox; Kelly Springell; Daniel J Hampshire; Moin D Mohamed; Martin McKibbin; Rowena Stern; F Lucy Raymond; Richard Sandford; Saghira Malik Sharif; Gulshan Karbani; Mustaq Ahmed; Jacquelyn Bond; David Clayton; Chris F Inglehearn
Journal:  Am J Hum Genet       Date:  2006-03-21       Impact factor: 11.025

Review 8.  The impact of recent population history on the deleterious mutation load in humans and close evolutionary relatives.

Authors:  Yuval B Simons; Guy Sella
Journal:  Curr Opin Genet Dev       Date:  2016-10-13       Impact factor: 5.578

9.  A gene for autosomal recessive symmetrical spastic cerebral palsy maps to chromosome 2q24-25.

Authors:  D P McHale; S Mitchell; S Bundey; L Moynihan; D A Campbell; C G Woods; N J Lench; R F Mueller; A F Markham
Journal:  Am J Hum Genet       Date:  1999-02       Impact factor: 11.025

10.  Human population structure, genome autozygosity and human health.

Authors:  Harry Campbell; Igor Rudan; Alan H Bittles; Alan F Wright
Journal:  Genome Med       Date:  2009-09-28       Impact factor: 11.117

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