Aliefendioğlu, DidemBademci, GülşahKeskil, S.Somuncu, SalihMısırlıoğlu, E.Çakmak, Ahmet Murat2020-06-252020-06-252007closedAccess1015-8146https://hdl.handle.net/20.500.12587/3999VACTERL-H associated with central hypothyroidism: A case report: The VACTERL-14 syndrome is a rare combination of vertebral anomalies, anal atresia, congenital heart defects, tracheo-esophageal fistula, abnormalities of kidneys and limb anomalies together with hydrocephalus. This condition is recognized as a hereditary entity with poor prognosis. We present a newborn weighing 3400 g, born by cesarean section to a 27 years old mother who had had an irregular antenatal follow-up. The patient had severe hydrocephalus, proximal esophageal atresia and distal tracheoesophageal fistula, gastric outlet obstruction, imperforated anus and recto-urethral fistula, patent ductus arterious, a bifid scrotum, a vertebral defect, sacral dimple and central hypothyroidism. The patient had no limb defects. The association of central hypothyroidism and VACTER-L-H has previously not been reported.eninfo:eu-repo/semantics/closedAccessVACTERL-Hhydrocephaluscentral hypothyroidismnewbornArticle1833313352-s2.0-3564902631618019375N/AWOS:000250607400009Q4