hereditary spastic paraplegia 36
MeSH: C567930ORPHA: 320365
Overview
hereditary spastic paraplegia that has material basis in variation in the chromosome region 12q23-q24
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 36, sourced from HPO and Orphanet clinical annotations.
HyperreflexiaLower limb spasticitySpastic gaitBabinski signProgressive spastic paraplegiaUrinary urgencyUrinary incontinenceDistal muscle weaknessProximal muscle weaknessImpaired distal proprioceptionImpaired distal vibration sensationImpaired distal tactile sensationDemyelinating motor neuropathyImpaired temperature sensationDemyelinating sensory neuropathyStrabismusArthritisPes cavus
Classification & Codes
MeSH Code
C567930Orphanet Code
ORPHA:320365hereditary spastic paraplegia 36
| MeSH | C567930 |
| Orphanet | ORPHA:320365 |
| Treatments | 0 drug(s) |
| Symptoms on record | 18 signs |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO