ORPHA:99857
Secondary syringomyelia
- Body system
- Neurological diseases
- Inheritance pattern
- Not documented in Orphadata
- Typical age of onset
- Adult
- Estimated prevalence
- Not documented in Orphadata
- Rarity class
- Not documented in Orphadata
ORPHA:99857 is classified under "Neurological diseases" in the Orphanet nomenclature.
Common signs
- Hyperintensity of MRI T2 signal of the spinal cord
- Gait disturbance
- Increased CSF protein concentration
- Paresthesia
- Back pain
- Fatigable weakness