Author/Authors :
Kaplan, Önder Süleyman Demirel Üniversitesi - Tip Fakültesi - Kadin Hastaliklari ve Dogum AD, Turkey , Güney, Mehmet Süleyman Demirel Üniversitesi - Tip Fakültesi - Kadin Hastaliklari ve Dogum AD, Turkey , Yüksel, Murat Süleyman Demirel Üniversitesi - Tip Fakültesi - Kadin Hastaliklari ve Dogum AD, Turkey
Title Of Article :
2. Trimester genetik tarama amniyosentez: 1586 olgunun degerlendirilmesi
Abstract :
Objective: The distribution of indications for amniocentesis attempts, rates by age, intervention methods, cell culture results are analyzed. Material and Methods: Amniocentesis performed for karyotyping in high risk pregnancies in department of Obstetrics and Gynecology, Suleyman Demirel University between 2003 and 2011 are investigated retrospectively. Results: 1586 cases are evaluated. Age of 19 24 8 % (132/1586), age of 25 30 13 % (217/1586), age of 31 35 % 24 (389/1586), age of 36 40 % 36 (574/1586), age of 41 44 % 17 (274/1586) was determined. 15-22 weeks of amniocentesis (17.2 ± 1.4) were made between. 3.65 % of chromosomal abnormalities (58/1586) of the patients had. Trisomy 21 (Down Syndrome) 1.1 % (18/1586) was determined. The patients with Down syndrome, 32 and 43years of age. 0,6 % (11/1586) pregnancy loss after amniocentesis. Conclusion: Genetic counseling is provided for all cases.
NaturalLanguageKeyword :
Amniocentesis , Genetic , Chromosomal Abnormality , Genetic Counseling
JournalTitle :
Medical Journal Of Suleyman Demirel University
