ORPHA:589827

Juvenile-onset Steinert myotonic dystrophy

Also called Juvenile-onset Steinert disease, Juvenile-onset myotonic dystrophy type 1

Body system

Neurological diseases

Inheritance pattern

Autosomal dominant

Typical age of onset

Childhood

Estimated prevalence

Unknown (Worldwide)

Rarity class

Unknown

ORPHA:589827 is classified under "Neurological diseases" in the Orphanet nomenclature.