hereditary spastic paraplegia 23
MeSH: C536859ORPHA: 101003
Overview
hereditary spastic paraplegia that has material basis in variation in the chromosome region 1q24-q32
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 23, sourced from HPO and Orphanet clinical annotations.
Multiple lentiginesVitiligoSpastic paraplegiaHyperreflexiaSpastic gaitWaddling gaitBowel incontinenceKyphoscoliosisBowel urgencyHorseshoe kidneySeizureSilver-gray hairHip dislocationShort stature
Classification & Codes
MeSH Code
C536859Orphanet Code
ORPHA:101003hereditary spastic paraplegia 23
| MeSH | C536859 |
| Orphanet | ORPHA:101003 |
| Treatments | 0 drug(s) |
| Symptoms on record | 14 signs |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO