Author/Authors :
Gezercan, Yurdal Çukurova Üniversitesi - Tıp Fakültesi - Beyin ve Sinir Cerrahisi Anabilim Dalı, Turkey , Özsoy, Kerem Mazhar Adana Numune Eğitim ve Araştırma Hastanesi - Beyin ve Sinir Cerrahisi Kliniği, Turkey , Oktay, Kadir Adana Numune Eğitim ve Araştırma Hastanesi - Beyin ve Sinir Cerrahisi Kliniği, Turkey , Çetinalp, Nuri Eralp Adana Numune Eğitim ve Araştırma Hastanesi - Beyin ve Sinir Cerrahisi Kliniği, Turkey , Erman, Tahsin Adana Numune Eğitim ve Araştırma Hastanesi - Beyin ve Sinir Cerrahisi Kliniği, Turkey , Zeren, Mustafa Yeni Hayat Hastanesi - Beyin ve Sinir Cerrahisi Kliniği, Turkey
Abstract :
Split cord malformations are rare form of occult spinal dysraphism in children. Split cord malformations are characterized by septum that cleaves the spinal canal in sagittal plane within the single or duplicated thecal sac. Although their precise incidence is unknown, split cord malformations are exceedingly rare and represent %3.8-5 of all congenital spinal anomalies. Characteristic neurological, urological, orthopedic clinical manifestations are variable and asymptomatic course is possible. Earlier diagnosis and surgical intervention for split cord malformations is associated with better long-term fuctional outcome. For this reason, diagnostic imaging is indicated for children with associated cutaneous and orthopedic signs. Additional congenital anomalies usually to accompany the split cord malformations. Earlier diagnosis, meticuolus surgical therapy and interdisciplinary careful evaluation and follow-up should be made for good prognosis.
NaturalLanguageKeyword :
Split cord malformation , spinal dysraphism , spina bifida , occult
