| Literature DB >> 26239489 |
Nihat Demir1, Erdal Peker2, İsmail Gülşen3, Kemal Ağengin4, Sultan Kaba5, Oğuz Tuncer2.
Abstract
Jarcho-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.Entities:
Keywords: Arnold–Chiari type 2; Jarcho–Levin syndrome; neural tube defect; newborn
Mesh:
Year: 2015 PMID: 26239489 DOI: 10.1177/0883073815596614
Source DB: PubMed Journal: J Child Neurol ISSN: 0883-0738 Impact factor: 1.987