Literature DB >> 14600825

Association of spondylocostal dysostosis and type I split cord malformation.

V Etus1, S Ceylan, S Ceylan.   

Abstract

In reports on children with congenital segmental costovertebral malformations who showed neural tube defects, cases with type I split cord malformation are quite rare. Up to now such association has been reported only in two cases with Jarcho-Levin syndrome. Here, a 7-year-old girl presenting with spondylocostal dysostosis and type I split cord malformation is reported. To the best of our knowledge, this is the first case documented in the literature. The association of segmental costovertebral malformations and neural tube defects is discussed. Genetic and embryological studies are also briefly reviewed.

Entities:  

Mesh:

Year:  2003        PMID: 14600825     DOI: 10.1007/s10072-003-0099-x

Source DB:  PubMed          Journal:  Neurol Sci        ISSN: 1590-1874            Impact factor:   3.307


  5 in total

1.  Split cord malformation types I and II: a personal series of 131 patients.

Authors:  Yusuf Erşahin
Journal:  Childs Nerv Syst       Date:  2013-09-07       Impact factor: 1.475

2.  Jarcho-Levin syndrome with diastematomyelia: A case report and review of literature.

Authors:  Ritesh Kansal; Amit Mahore; Sanjay Kukreja
Journal:  J Pediatr Neurosci       Date:  2011-07

3.  Spondylocostal dysostosis with lipomyelomeningocele: Case report and review of the literature.

Authors:  Shailendra D Anjankar; Raju Subodh
Journal:  J Pediatr Neurosci       Date:  2014 Sep-Dec

4.  Spondylocostal dysostosis (Jarcho-Levine syndrome) associated with occult spinal dysraphism: Report of two cases.

Authors:  Natarajan Muthukumar
Journal:  J Pediatr Neurosci       Date:  2015 Apr-Jun

5.  Rare association of spondylo costal dysostosis with split cord malformations type II: A case report and a brief review of literature.

Authors:  Bhavanam Hanuma Srinivas; Aneel Kumar Puligopu; Dinesh Sukhla; Prajnya Ranganath
Journal:  J Pediatr Neurosci       Date:  2014-05
  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.