ORPHA:238455

Infantile dystonia-parkinsonism

Also called DTDS, Dopamine transporter deficiency syndrome, IPD, PKDYS

Body system

Neurological diseases

Inheritance pattern

Autosomal recessive

Typical age of onset

Infancy, Neonatal

Estimated prevalence

<1 / 1 000 000 (Worldwide)

Rarity class

<1 / 1 000 000

ORPHA:238455 is classified under "Neurological diseases" in the Orphanet nomenclature.