Rare Zebra

Rare disease search prototype built on Orphanet data

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ORPHA:438266

Progressive encephalomyelitis with rigidity and myoclonus

Also called PERM

Body system
Neurological diseases
Inheritance pattern
Not applicable
Typical age of onset
Adult, Infancy
Estimated prevalence
Unknown (Europe)
Rarity class
Unknown

ORPHA:438266 is classified under "Neurological diseases" in the Orphanet nomenclature.

Common signs