Central Asian Journal of Medicine


Determination of the frequency of individual anatomical variants, their clinical and neurological manifestations and evaluation of the effectiveness of complex treatment of children with the syndrome of fixed spinal cord in osteoneural anomalies of the spine and spinal cord. 156 (48.6%) boys and 165 (51.4%) girls aged from one day to 18 years with concealed spinal dysraphism of various forms in combination with other types of spinal malformations were analyzed. In the genesis of residual and progressive neurological disorders in children after operations for spinal malformations, the leading role plays “fixed spinal cord” syndrome of in the form of congenital pathology of innate character before surgery or adhesive process associated with surgical intervention. The most common causes of “fixed spinal cord” syndrome are the latent spinal dysraphism of congenital genesis (lipomielocele, diastomatomyelia, syringomyelia, hydromyelia) and the phenomenon of secondary spinal cord fixation syndrome that arise after the operation.

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