parkinsonism-dystonia, infantile

The information provided on this page is for informational purposes only. The National Organization for Rare Disorders (NORD) does not endorse the information presented. The content has been gathered in partnership with the MONDO Disease Ontology. Please consult with a healthcare professional for medical advice and treatment.

Print

Disease Overview

Infantile dystonia-parkinsonism (IPD) is an extremely rare inherited neurological syndrome that presents in early infancy with hypokinetic parkinsonism and dystonia and that can be fatal.


Synonyms

  • IPD
  • PARKINSONISM-dystonia, infantile
  • PKDYS
  • Parkinsonism-dystonia infantile
  • dopamine transporter deficiency syndrome
  • infantile Parkinsonism-dystonia
  • parkinsonism-dystonia, infantileIPD
  • PARKINSONISM-dystonia, infantile
  • PKDYS
  • Parkinsonism-dystonia infantile
  • dopamine transporter deficiency syndrome
  • infantile Parkinsonism-dystonia
  • parkinsonism-dystonia, infantile