hereditary spastic paraplegia 41
ORPHA: 320355
Overview
hereditary spastic paraplegia that has material basis in variation in the chromosome region 11p14.1-p11.2
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 41, sourced from HPO and Orphanet clinical annotations.
HyperreflexiaLower limb spasticitySpastic gaitDegeneration of the lateral corticospinal tractsProgressive spastic paraplegiaUrinary urgencyProximal muscle weaknessLower limb amyotrophyHand muscle weaknessSpinal cord lesion
Classification & Codes
Orphanet Code
ORPHA:320355hereditary spastic paraplegia 41
| Orphanet | ORPHA:320355 |
| Treatments | 0 drug(s) |
| Symptoms on record | 10 signs |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO