autosomal recessive complex spastic paraplegia type 9B
ORPHA: 447760
Overview
human disease
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 autosomal recessive complex spastic paraplegia type 9B, sourced from HPO and Orphanet clinical annotations.
SpasticityLower limb hyperreflexiaBabinski signUpper limb hyperreflexiaDysarthriaMotor delayMuscle weaknessGrowth delaySpastic gaitPostural tremorTetraplegiaImpaired continenceUrinary retentionMicrocephalyDelayed speech and language developmentGlobal developmental delayAbnormal facial shapeCerebral cortical atrophyLoss of speechPrimitive reflexAbnormal periventricular white matter morphologyKyphoscoliosisSkeletal muscle atrophyAbsent Achilles reflexShort statureImpaired vibration sensation at anklesCorpus callosum atrophyTip-toe gaitPollakisuria
Classification & Codes
Orphanet Code
ORPHA:447760autosomal recessive complex spastic paraplegia type 9B
| Orphanet | ORPHA:447760 |
| Treatments | 0 drug(s) |
| Symptoms on record | 29 signs |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO