Parkinsonian-pyramidal syndrome
MeSH: C538104ORPHA: 171695
Overview
Parkinson's disease that has material basis in mutation in the FBXO7 gene on chromosome 22q12.3
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 Parkinsonian-pyramidal syndrome, sourced from HPO and Orphanet clinical annotations.
ParkinsonismAbnormal pyramidal signNeurogenic bladderHypomimic faceSlow saccadic eye movementsSpasticityDystoniaMyoclonusHyperreflexiaTalipes equinovarusDysphagiaRigidityBradykinesiaIntention tremorPostural instabilitySleep disturbanceShuffling gaitVisual hallucinationBabinski signSubstantia nigra gliosisAbnormal autonomic nervous system physiologyMonotonic speechCognitive impairmentDementiaLewy bodies
Classification & Codes
MeSH Code
C538104Orphanet Code
ORPHA:171695Parkinsonian-pyramidal syndrome
| MeSH | C538104 |
| Orphanet | ORPHA:171695 |
| Treatments | 0 drug(s) |
| Symptoms on record | 25 signs |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO