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Spinal Cord Lateral Hemisection and Asymmetric Behavioral Assessments in Adult Rats
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Widely separated composite split cord malformation.

Deepak Kumar Singh1, Neha Singh, Ragini Singh

  • 1Department of Neurosurgery, Dr. RMLIMS, Lucknow, Uttar Pradesh, India.

BMJ Case Reports
|October 5, 2012
PubMed
Summary
This summary is machine-generated.

This report details a rare case of split cord malformations (SCMs) in an 18-month-old child affecting two distinct spinal regions. Such widely separated SCMs are infrequently documented in medical literature.

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Area of Science:

  • Pediatric Neurology
  • Developmental Biology
  • Spinal Cord Anomalies

Background:

  • Split cord malformation (SCM) is a rare congenital anomaly involving the division of the spinal cord.
  • SCMs typically occur as a single event, with varying locations along the spinal axis.
  • Understanding the embryological basis of SCM is crucial for diagnosing and managing these complex conditions.

Observation:

  • An 18-month-old child presented with split cord malformations (SCMs).
  • The SCMs were identified at two distinct and widely separated levels: the upper thoracic (T2) and lumbar (L2) regions.
  • This dual-level occurrence represents a rare anatomical variation.

Findings:

  • The case highlights the possibility of split cord malformations occurring at multiple, distant spinal cord levels.
  • Radiological and clinical findings confirmed the presence of SCMs at both T2 and L2.
  • The rarity of this specific presentation (wide separation) is emphasized, with few similar cases reported.

Implications:

  • This case expands the known spectrum of split cord malformation presentations.
  • It underscores the importance of thorough spinal imaging in pediatric patients with suspected congenital anomalies.
  • Further research into the developmental mechanisms underlying multiple SCMs may be warranted.