NIH GARD Information: Spastic paraplegia 23
This information is provided by the National Institutes of Health (NIH)
Genetic and Rare Diseases Information Center (GARD).
- SPG 23
- Spastic paraplegia and pigmentary abnormalities
- Spastic paraplegia vitiligo premature graying and characteristic facies
- Lison syndrome
- Autosomal recessive spastic paraplegia type 23
No overview is available at this time. Please check back for future updates.
For more information, visit GARD.