ORPHA:500

Noonan syndrome with multiple lentigines

Also called Cardiomyopathic lentiginosis, Familial multiple lentigines syndrome, LEOPARD syndrome

Body system

Skin diseases

Inheritance pattern

Autosomal dominant

Typical age of onset

Neonatal

Estimated prevalence

<1 / 1 000 000 (Worldwide)

Rarity class

<1 / 1 000 000

ORPHA:500 is classified under "Skin diseases" in the Orphanet nomenclature.