EVIDENCE FOR GENETIC-CONTROL OF NONDISJUNCTION IN MAN

  • 1 January 1980
    • journal article
    • research article
    • Vol. 32  (4) , 477-483
Abstract
Data on factors associated with the occurrence of Down syndrome in a highly inbred population were evaluated to investigate the presence of a genetic control of nondisjunction in man. In Kuwait, close consanguinity occurs in 40% of marriages. In its main obstetric hospital, 20 trisomic Down babies out of 11,614 singleton births were delivered over 12 mo. Chi-square analyses indicate the occurrence of Down syndrome to be linked to 2 independent factors: consanguinity of parents and maternal age. The relative risk is .apprx. 4 .times. greater for closely related parents than for nonrelated (P < 0.005); a possible explanation for this is the existence of a gene that induces mitotic nondisjunction in the homozygous fertilized ovum. An alternative explanation is the existence of an autosomal recessive gene which results in meiotic nondisjunction in the homozygous parents. Consanguinity is usually perpetuated in certain families, or sections of the population, and parents in highly inbred families have a higher probability to be homozygotes for that gene.

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