
PRENATAL DIAGNOSIS OF TRANSLOCATION 13;13
PATAU SYNDROME: CLINICAL FEATURES OF TWO CASES Pazarbaþi A1,*, Demirhan O1, Süleymanova-Karahan D1,Taþtemir D1,
Tunç E1, Gümürdülü D2 *Corresponding Author: Ayfer Pazarbaþi, Ph.D., Department of Medical Biology and Genetics,
School of Medicine, Çukurova University, 01330 Balcali, Adana, Turkey; Tel.: +90-322-338-70-
68; Fax: +90-322-338-65-72; E-mail: payfer@cu.edu.tr page: 69
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MATERIALS AND METHODS
The two cases described here were diagnosed with abnormal USG (ultra sonography) findings at the Department of Gynecology and Obstetrics, Faculty of Medicine, Çukurova University, Adana, Turkey. Chromosomal analyses of cord blood, peripheral blood lymphocytes and of amniotic fluid cells were performed according to standard cytogenetic methods using a G-banding technique. Lymphocytes were cultured in RPMI 1640 (Sigma-Aldrich Inc., Munich, Germany). Chromosome slides were made according to routine procedures [11]. Twenty metaphases of each individual were examined for chromosomal aberrations after solid Giemsa staining and were recorded according to the International System for Human Cyto genetic Nomenclature [12]. Chromosomes were photographed, destained, and subseguently GTG-banded (G bands by trypsin using Giemsa) for evaluation. Histopa thologically examined features were described for the two fetuses.
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