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Chromosomal Abnormalities Through Amniocentesis
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نویسنده
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pourahmad aghdas ,saadati nasrin ,barati mojgan ,moramezi farideh ,mohamadjafari razieh
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منبع
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jentashapir journal of cellular and molecular biology - 2019 - دوره : 10 - شماره : 2 - صفحه:1 -3
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چکیده
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Objectives: the study aimed to assess the frequency and type of abnormal karyotype in khuzestan, iran by amniocentesis before 22 weeks of gestation. methods:we conducted a retrospective analysis of 1197 amniotic fluid specimens in khuzestan province, before 22 weeks gestations for fetal karyotyping. results: the incidence of abnormal aneuploidies was 4.9% (59 of 1197) for all specimens. the highest chromosomal abnormality was down syndrome (64.4%). conclusions: the rate of chromosomal abnormalities was higher than other reports from iran and all over the world. the detection rate of down syndrome similar to other reports remains high.
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کلیدواژه
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Chromosomal Abnormalities ,Amniocentesis ,Down Syndrome ,Second Trimester
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آدرس
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ahvaz jundishapur university of medical sciences, fertility,infertility and perinatology research center, iran, ahvaz jundishapur university of medical sciences, school of medicine, fertility, infertility and perinatology research center, department of social medicine, Iran, ahvaz jundishapur university of medical sciences, fertility,infertility and perinatology research center, iran, ahvaz jundishapur university of medical sciences, fertility,infertility and perinatology research center, iran, ahvaz jundishapur university of medical sciences, fertility,infertility and perinatology research center, iran
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پست الکترونیکی
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rmj417072@gmail.com
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Authors
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