Demir, NihatPeker, ErdalGulsen, IsmailAgengin, KemalKaba, SultanTuncer, Oguz2025-05-102025-05-1020160883-07381708-828310.1177/08830738155966142-s2.0-84957942506https://doi.org/10.1177/0883073815596614https://hdl.handle.net/20.500.14720/14946Ayengin, Kemal/0000-0002-1633-3200; Demir, Nihat/0000-0003-3287-7221Jarcho-Levin syndrome (JLS) is a genetic disorder characterized by distinct malformations of the ribs and vertebrae, and/or other associated abnormalities such as neural tube defect, Arnold-Chiari malformation, renal and urinary abnormalities, hydrocephalus, congenital cardiac abnormalities, and extremity malformations. The study included 12 cases at 37-42 weeks of gestation and diagnosed to have had Jarcho-Levin syndrome, Arnold-Chiari malformation, and meningmyelocele. All cases of Jarcho-Levin syndrome had Arnold-Chiari type 2 malformation; there was corpus callosum dysgenesis in 6, lumbosacral meningmyelocele in 6, lumbal meningmyelocele in 3, thoracal meningmyelocele in 3, and holoprosencephaly in 1 of the cases. With this article, the authors underline the neurologic abnormalities accompanying Jarcho-Levin syndrome and that each of these abnormalities is a component of Jarcho-Levin syndrome.eninfo:eu-repo/semantics/openAccessJarcho-Levin SyndromeNeural Tube DefectArnold-Chiari Type 2NewbornArticle314Q3Q241542026239489WOS:000370719900002