Alp, E.Alp, H.Atabek, M. E.Pirgon, Ö.2020-03-262020-03-2620101308-5727https://dx.doi.org/10.4274/jcrpe.v2i1.49https://hdl.handle.net/20.500.12395/25578Al-Awadi/Raas-Rothschild (AARR) syndrome is a rare phocomelia syndrome characterized by limb/pelvic hypoplasia/aplasia, renal anomalies such as horseshoe and polycystic kidney, and abnormal facial features including cleft palate, hypertelorism and micro-retrognatia. Autosomal recessive inheritance has been proposed for AARR syndrome. In this report a boy affected with AARR syndrome is presented. The previous pregnancy of the mother was terminated because of lower limb agenesis detected at 14 th week of gestation. This report emphasizes the importance of recognizing severe pelvic and limb deficiencies in newborns with AARR syndrome and differentiating the syndrome from other multiple malformation syndromes. Fetal ultrasonography at 15 th week of gestation is helpful in diagnosing the major extremity anomalies in the fetus. © Journal of Clinical Research in Pediatric Endocrinology, Published by Galenos Publishing.en10.4274/jcrpe.v2i1.49info:eu-repo/semantics/openAccessAl-Awadi/Raas-Rothschild syndromePelvic agenesisPhocomeliaArticle21495121274338Q2