Ornek, NurgulOgurel, ReyhanOrnek, Kemal2020-06-252020-06-252016closedAccess1381-68101744-5094https://doi.org/10.3109/13816810.2014.902079https://hdl.handle.net/20.500.12587/6647Ornek, Nurgul/0000-0003-3068-1831Rieger syndrome (RS) is a multiple malformation syndrome characterized by ocular manifestations and extraocular defects. Herein, we report a 9-year-old boy who exhibited Rieger Syndrome phenotype as well as congenital hypothyroidism which may be an underappreciated feature of RS.eninfo:eu-repo/semantics/closedAccessCongenitalhypothyroidismRieger SyndromeArticle371868810.3109/13816810.2014.9020792-s2.0-8496041879824666291Q2WOS:000371921400014Q4