ORPHA:589824

Childhood-onset Steinert myotonic dystrophy

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

Body system

Neurological diseases

Inheritance pattern

Autosomal dominant

Typical age of onset

Childhood, Infancy

Estimated prevalence

Unknown (Worldwide)

Rarity class

Unknown

ORPHA:589824 is classified under "Neurological diseases" in the Orphanet nomenclature.