hereditary spastic paraplegia 72
ORPHA: 401849
Overview
hereditary spastic paraplegia that has material basis in mutation in the REEP2 gene on chromosome 5q31
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 72, sourced from HPO and Orphanet clinical annotations.
RigiditySpastic gaitPes cavusUrinary bladder sphincter dysfunctionPostural tremorMemory impairmentImpaired vibration sensation at anklesAbnormality of mental functionPain
Classification & Codes
Orphanet Code
ORPHA:401849hereditary spastic paraplegia 72
| Orphanet | ORPHA:401849 |
| Treatments | 0 drug(s) |
| Symptoms on record | 9 signs |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO