@article{Nergiz_Demircan Sezer_Altınkaya_Küçük_Yüksel_2014, place={Ankara, TR}, title={Meckel Gruber Syndrome- A Case Report And Review of Literature}, volume={20}, url={https://www.gorm.com.tr/index.php/GORM/article/view/169}, abstractNote={<p>Meckel-Gruber syndrome (MGS) is a lethal autosomal recessive disorder. MGS is thought to be caused by ciliary dysfunction. The worldwide incidence of MGS varies from 1 in 13 250 to 1 in 140.000 live births. MGS is characterized by three main symptoms: central nervous system (CNS) malformations, tetramelic postaxial polydactyly and cystic renal dysplasia with associated fibrocystic changes of the liver, pancreas and epididymis. Here a case of MG syndrome, diagnosed in early weeks of gestation was reported.</p>}, number={3}, journal={Gynecology Obstetrics & Reproductive Medicine}, author={Nergiz, Sümeyra and Demircan Sezer, Selda and Altınkaya, Sündüz Özlem and Küçük, Mert and Yüksel, Hasan}, year={2014}, month={Dec.}, pages={175–177} }