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Issue title: Spina Bifida, Part 2
Article type: Research Article
Authors: Al-Holou, Wajd N. | Garton, Hugh J.L. | Muraszko, Karin M. | Maher, Cormac O.
Affiliations: Department of Neurosurgery, University of Michigan, Ann Arbor, MI, USA
Note: [] Address for correspondence: Cormac O. Maher, M.D., Department of Neurosurgery, University of Michigan, 3552 Taubman Center, 1500 East Medical Center Drive, Ann Arbor, MI 48109-0338, USA. Tel.: +1 734 615 0536; E-mail: cmaher@med.umich.edu
Abstract: Myelomeningocele is associated with other neurological abnormalities, including hydrocephalus, Chiari II malformations, syringomyelia, and secondary tethered cord syndrome. Tethered cord syndrome occurs because of abnormal attachment of the spinal cord to the caudal dural sac, causing cord ischemia. Occasionally, symptoms of progressive neurological deterioration may occur and can significantly affect the long-term outcome of these patients. Proper management of patients with myelomeningocele requires long-term follow-up and evaluation of signs of neurological deterioration that suggest secondary tethered cord syndrome. Treatment of these patients may target symptoms, such as urological intervention for bladder dysfunction, or it may target the tethered cord itself. Recently, many studies have shown that tethered cord release can significantly improve symptoms in these patients.
Keywords: Myelomeningocele, tethered spinal cord, retethering, tethered cord release, pediatric neurosurgery
DOI: 10.3233/PRM-2009-0060
Journal: Journal of Pediatric Rehabilitation Medicine, vol. 2, no. 1, pp. 29-36, 2009
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