Diastematomyelia is a rare congenital malformation of the spinal canal in which parts of the spinal cord are divided longitudinally.
Embryology
The exact embryological cause of the development of diastematomyelia is unknown1.
Classification
Diastematomyelia is classified according to the Pang classification.
Treatment
Surgical treatment may be indicated if clinical neurological symptoms consistent with tethered cord develop.
References