Kilinç N.Etem H.2024-04-242024-04-2420071016-5126https://hdl.handle.net/11468/24225Fraser 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 central nervous system. Renal anomalies (uni-or bilateral agenesis) occur in 85 per cent. These anomalies were first documented by Fraser in 1962. Two Fraser syndrome cases diagnosed as normal spontan vaginal post delivery without prenatal following were presented rarely in the light of the literature knowledge.trinfo:eu-repo/semantics/closedAccessAutopsyCryptophthalmosFraser SyndromeSyndactylyArticle21159622-s2.0-34347373729N/A