Abstract
Myelomeningocele is the most common neural tube defect and it is the most severe birth defect that is compatible with survival. In the early 1950’s, the survival rate for the patients with myelomeningocele was about 10 percent. Today, large numbers of children with myelomeningocele are surviving into adulthood because of recent advances in the management of several important complications and monitorization of the nörological complications gains importance with the prerequisite of improving quality of life. Deterioration of clinical manifestations can be caused by undiagnosed shunt malfunction, progression of Chiari II symptoms, hydromyelia, and tethered cord syndrome, as well as orthopedic and urological complications. Optimal treatment requires specialized care to prevent, monitor, and treat a variety of potential complications that can affect neurological functions, quality of life, and survival of the patients. This care is ideally provided by a multidisciplinary team with expertise in pediatric subspecialties of neurosurgery, orthopedics, neurology, urology, and rehabilitation.
Keywords: Myelomeningocele, neural tube defect, tethered cord, management
Copyright and license
Copyright © 2014 The Author(s). This is an open access article distributed under the Creative Commons Attribution License (CC BY), which permits unrestricted use, distribution, and reproduction in any medium or format, provided the original work is properly cited.