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Sadik Zbair1, Asmaa Adnane1, Kamilia Chbani1

  • 1Université Hassan II, Faculté de Médecine et de Pharmacie, Service de Radiologie Pédiatrique, Hôpital Abderrahim Harouchi, CHU IBN Rochd, Casablanca, Maroc.

The Pan African Medical Journal
|May 4, 2018
PubMed
Summary

This case report details diastematomyelia, a rare spinal cord malformation, in a 12-year-old male. MRI revealed type 1 diastematomyelia with associated tethered cord, syringomyelia, neuroenteric cyst, and dermal sinus.

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Area of Science:

  • Neurology
  • Radiology
  • Pediatric Surgery

Background:

  • Diastematomyelia is a rare congenital spinal anomaly characterized by the longitudinal splitting of the spinal cord.
  • It is a type of spinal dysraphism, often associated with other vertebral and neural malformations.
  • Two types of diastematomyelia are recognized, distinguished by the presence or absence of a bony septum.
Keywords:
Diastematomyelianeural tube defectsspinal dysraphism

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