ORPHA:210141
Inherited congenital spastic tetraplegia
Also called Inherited congenital spastic quadriplegia
- Body system
- Neurological diseases
- Inheritance pattern
- Autosomal recessive, Unknown
- Typical age of onset
- Infancy, Neonatal
- Estimated prevalence
- <1 / 1 000 000 (Worldwide)
- Rarity class
- <1 / 1 000 000
ORPHA:210141 is classified under "Neurological diseases" in the Orphanet nomenclature.