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Genetic referrals of Middle Eastern origin in a western city: inbreeding and disease profile.
Hoodfar, E; Teebi, A S.
Afiliação
  • Hoodfar E; F Clarke Fraser Clinical Genetics Unit, Montreal Children's Hospital and McGill University, Canada.
J Med Genet ; 33(3): 212-5, 1996 Mar.
Article em En | MEDLINE | ID: mdl-8728693
ABSTRACT
Inbreeding or consanguineous marriage is a common traditional practice in Middle Eastern cultures. Studies from various countries and communities of this region showed that the frequencies range from 20% to greater than 70%. Inbreeding is known to have adverse effects on morbidity and mortality, in particular with respect to autosomal recessive disorders. This study examined 200 couples representing all referrals of Middle Eastern origin seen at a large Clinical Genetics Unit in Montreal. They were compared with a similar sized group of different cultural backgrounds from among the same referrals. The rate of intercultural marriages and inbreeding was found to be 24% and 23.5% respectively in the Middle Eastern group, while they were 22.5% and 5% in the comparison group. Excluding the referrals for consanguinity only, the rate of inbreeding among the study group was 16.4%. Within the Middle Eastern group, autosomal recessive disorders were more than twice as common in the inbred than in the non-inbred families, the pattern of which is consistent with previous observations.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Consanguinidade / Doenças Genéticas Inatas Tipo de estudo: Incidence_studies / Prognostic_studies Limite: Female / Humans / Male País/Região como assunto: America do norte / Asia Idioma: En Revista: J Med Genet Ano de publicação: 1996 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Consanguinidade / Doenças Genéticas Inatas Tipo de estudo: Incidence_studies / Prognostic_studies Limite: Female / Humans / Male País/Região como assunto: America do norte / Asia Idioma: En Revista: J Med Genet Ano de publicação: 1996 Tipo de documento: Article