hereditary spastic paraplegia 14
MeSH: C537486ORPHA: 100995
Overview
hereditary spastic paraplegia that has material basis in variation in the chromosome region 3q27-q28
Available Treatments (0)
No treatments linked yet
Clinical trials or compassionate use may be available — consult a specialist.
Clinical Presentation
Signs and symptoms associated with hereditary spastic paraplegia 14, sourced from HPO and Orphanet clinical annotations.
Mild intellectual disabilityHyperreflexiaPes cavusSpastic gaitBabinski signLower limb hypertoniaMotor axonal neuropathy
Classification & Codes
MeSH Code
C537486Orphanet Code
ORPHA:100995hereditary spastic paraplegia 14
| MeSH | C537486 |
| Orphanet | ORPHA:100995 |
| Treatments | 0 drug(s) |
| Symptoms on record | 7 signs |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO