YYÜ GCRIS Basic veritabanının içerik oluşturulması ve kurulumu Research Ecosystems (https://www.researchecosystems.com) tarafından devam etmektedir. Bu süreçte gördüğünüz verilerde eksikler olabilir.
 

A Single-Center Experience of Cns Anomalies or Neural Tube Defects in Patients With Jarcho-Levin Syndrome

dc.authorid Ayengin, Kemal/0000-0002-1633-3200
dc.authorid Demir, Nihat/0000-0003-3287-7221
dc.authorscopusid 55598145000
dc.authorscopusid 26025132600
dc.authorscopusid 54895174500
dc.authorscopusid 57113719700
dc.authorscopusid 55570979200
dc.authorscopusid 56186063400
dc.authorwosid Ayengin, Kemal/Abi-4555-2020
dc.authorwosid Demi̇r, Ni̇hat/Gry-3625-2022
dc.contributor.author Demir, Nihat
dc.contributor.author Peker, Erdal
dc.contributor.author Gulsen, Ismail
dc.contributor.author Agengin, Kemal
dc.contributor.author Kaba, Sultan
dc.contributor.author Tuncer, Oguz
dc.date.accessioned 2025-05-10T17:39:37Z
dc.date.available 2025-05-10T17:39:37Z
dc.date.issued 2016
dc.department T.C. Van Yüzüncü Yıl Üniversitesi en_US
dc.department-temp [Demir, Nihat; Peker, Erdal; Tuncer, Oguz] Yuzuncu Yil Univ, Sch Med, Dept Pediat, Div Neonatol, TR-65100 Van, Turkey; [Gulsen, Ismail] Yuzuncu Yil Univ, Sch Med, Dept Neurosurg, TR-65100 Van, Turkey; [Agengin, Kemal] Yuzuncu Yil Univ, Sch Med, Dept Pediat Surg, TR-65100 Van, Turkey; [Kaba, Sultan] Yuzuncu Yil Univ, Sch Med, Dept Pediat, TR-65100 Van, Turkey en_US
dc.description Ayengin, Kemal/0000-0002-1633-3200; Demir, Nihat/0000-0003-3287-7221 en_US
dc.description.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. en_US
dc.description.woscitationindex Science Citation Index Expanded
dc.identifier.doi 10.1177/0883073815596614
dc.identifier.endpage 420 en_US
dc.identifier.issn 0883-0738
dc.identifier.issn 1708-8283
dc.identifier.issue 4 en_US
dc.identifier.pmid 26239489
dc.identifier.scopus 2-s2.0-84957942506
dc.identifier.scopusquality Q2
dc.identifier.startpage 415 en_US
dc.identifier.uri https://doi.org/10.1177/0883073815596614
dc.identifier.uri https://hdl.handle.net/20.500.14720/14946
dc.identifier.volume 31 en_US
dc.identifier.wos WOS:000370719900002
dc.identifier.wosquality Q3
dc.language.iso en en_US
dc.publisher Sage Publications inc en_US
dc.relation.publicationcategory Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı en_US
dc.rights info:eu-repo/semantics/openAccess en_US
dc.subject Jarcho-Levin Syndrome en_US
dc.subject Neural Tube Defect en_US
dc.subject Arnold-Chiari Type 2 en_US
dc.subject Newborn en_US
dc.title A Single-Center Experience of Cns Anomalies or Neural Tube Defects in Patients With Jarcho-Levin Syndrome en_US
dc.type Article en_US

Files