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- W2320118904 abstract "Fetal chromosomal and structural abnormalities are one of major causes of perinatal mortality and morbidity. Screening for fetal chromosomal and structural abnormalities is an important part of prenatal care today in the parts of the world where economical situation permit it. Today, first trimester biochemical and ultrasound screening is “gold standard” in prenatal care in many countries in Europe and other parts of the world. If done in a standardized way, it permits high detection of chromosomal and structural fetal anomalies between 11-14 gestational weeks. Pre and post-test counseling must be available for all pregnant women. The aims of second trimester scans, which are performed between 18 and 24 week of gestation, are to determine fetal biometry and anatomy, to detect structural abnormalities and (re)assess risk for chromosomal abnormalities by checking for soft markers and to asses risk for preterm delivery by measuring cervix of the uterus and for preecplampsia by assessment of uterine arteries Doppler." @default.
- W2320118904 created "2016-06-24" @default.
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- W2320118904 date "2015-01-01" @default.
- W2320118904 modified "2023-10-18" @default.
- W2320118904 title "SCREENING TESTS FOR FETAL CHROMOSOMAL AND STRUCTURAL ABNORMALITIES" @default.
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- W2320118904 doi "https://doi.org/10.5644/pi2015-159.03" @default.
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