Kilinc, NihalDemir, SureyyaDemir, Bulent2025-01-272025-01-2720151302-00722147-2688https://doi.org/10.4274/haseki.2503https://hdl.handle.net/20.500.12428/28790Fraser syndrome (cryptophthalmos syndactyly syndrome) is a rare autosomal recessive disorder. The main features are cryptophthalmos (hidden eye), ear, nose and skeletal malformations, syndactyly, laryngeal stenosis and malformation of the uro-genital system, lungs, liver, and the central nervous system. Renal anomalies (unilateral/bilateral agenesis) occur in 85% of cases. These anomalies were first documented by Fraser in 1962. In this paper, we present two cases of Fraser syndrome diagnosed after a normal spontaneous vaginal delivery without prenatal follow-up in the light of the literature.trinfo:eu-repo/semantics/openAccessFraser syndromecryptophthalmossyndactylyautopsyArticle53327327610.4274/haseki.2503N/AWOS:0002167555000232-s2.0-84941558048Q3