ORPHA:623626
Paraneoplastic cerebellar degeneration
Also called PCD, Paraneoplastic cerebellar ataxia, Rapidely progressive cerebellar syndrome, Subacute cerebellar degeneration
- Body system
- Neurological diseases
- Inheritance pattern
- Not applicable
- Typical age of onset
- All ages
- Estimated prevalence
- 1-9 / 1 000 000 (Europe)
- Rarity class
- 1-9 / 1 000 000
ORPHA:623626 is classified under "Neurological diseases" in the Orphanet nomenclature.
Common signs
- CSF oligoclonal immunoglobulin G bands
- Ataxia
- Increased CSF protein concentration
- CSF pleocytosis
- Nystagmus
- Diplopia