cytogenetic stidy of 366 affected children with down’s syndrome in iran
نویسندگان
چکیده
down’s syndrome, or 21 trisomy, is the most common autosomal abnormality, with incidence of 1 per 815 live births in iran. worldwide reports indicate that about 95% are regular trisomy, or nondisjunction, 1% are mosaic and 4% due to translocation. however, these values show a geographical variation. a cytogenetic study of down's syndrome, or trismoy 21, was carried out on 366 cases (202 males and 164 females) during a 10 year period (1974-1983) in akbarabadi maternity hospital in tehran. the lymphocyte chromosomes were stained with g-banding technique. free trisomy 21 constituted 93.44%, d/g translocation 3.55% and g/g translocation 3.01%. reciprocal translocation and mosaic were not observed. the values are compared with other studies in some of the countries of the countries of the region.
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Background Down syndrome is the most common chromosomal anomaly. Dysmorphic features can occur in several organs in this syndrome. Cardiac anomalies with a prevalence of 50% are the most common anomalies responsible for death during the first two years of life. We aimed to determine the prevalence of cardiac anomalies among Down syndrome patients admitted to two tertiary hospitals in Kermanshah...
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عنوان ژورنال:
iranian journal of public healthجلد ۲۵، شماره ۳-۴، صفحات ۱-۴
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