ORPHA:820

Sneddon syndrome

Also called Ehrmann-Sneddon syndrome, Livedo racemosa-cerebrovascular accident syndrome, Livedo reticularis-cerebrovascular accident syndrome

Body system

Neurological diseases

Inheritance pattern

Autosomal dominant, Not applicable

Typical age of onset

Adult

Estimated prevalence

1-9 / 1 000 000 (Europe)

Rarity class

1-9 / 1 000 000

ORPHA:820 is classified under "Neurological diseases" in the Orphanet nomenclature.