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Split spinal cord malformation.

R Shane Tubbs1, E George Salter, W Jerry Oakes

  • 1Section of Pediatric Neurosurgery, Children's Hospital, Birmingham, Alabama, USA. rstubbs@uab.edu

Clinical Anatomy (New York, N.Y.)
|November 23, 2005
PubMed
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This study details a rare case of split cord malformation, a congenital spinal anomaly, in a young girl. The findings highlight a Type I split cord malformation with bony septation, emphasizing its unique presentation and embryological considerations.

Area of Science:

  • Neurology
  • Developmental Biology
  • Pediatric Surgery

Background:

  • Split cord malformation is a rare congenital anomaly of the spine.
  • Spinal dysraphism encompasses a spectrum of developmental abnormalities.

Observation:

  • A case of split cord malformation was identified in a young female patient.
  • The anomaly was classified as Type I, characterized by midline bony septation.

Findings:

  • The Type I split cord malformation was isolated, with no other associated pathologies.
  • The embryology and clinical manifestations of this spinal anomaly are reviewed.

Implications:

  • Understanding the embryogenesis of split cord malformation is crucial for diagnosis.

Related Experiment Videos

  • This case contributes to the literature on rare congenital spinal conditions.
  • Further research into clinical management strategies for split cord malformation is warranted.