idiopathic camptocormia
MeSH: C537968ORPHA: 1320
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 idiopathic camptocormia, sourced from HPO and Orphanet clinical annotations.
Abnormality of the nervous systemDystoniaCerebral atrophyAbnormal cerebral white matter morphologyOsteoarthritisEMG: neuropathic changesEMG: myopathic abnormalitiesAbnormal intervertebral disk morphologyEMG: impaired neuromuscular transmissionAbnormality of the headParkinsonismElevated circulating creatine kinase concentrationEMG: chronic denervation signsProximal spinal muscular atrophyAmyotrophic lateral sclerosisAbnormal inflammatory responseAbnormality of movementAbnormal basal ganglia morphologyFrontotemporal dementiaMyotoniaAlzheimer diseaseAbnormality of the immune systemSyringomyeliaAbnormal synaptic transmission at the neuromuscular junctionSpinal canal stenosisMitochondrial myopathyAbnormal pons morphologyMyelitisFatty replacement of skeletal muscleAbnormal muscle fiber dysferlinFatigable weakness of skeletal musclesLewy bodiesMyositis
Classification & Codes
MeSH Code
C537968Orphanet Code
ORPHA:1320idiopathic camptocormia
| MeSH | C537968 |
| Orphanet | ORPHA:1320 |
| Treatments | 0 drug(s) |
| Symptoms on record | 33 signs |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO