ORPHA:352649
Brain dopamine-serotonin vesicular transport disease
- Body system
- Inborn errors of metabolism
- Inheritance pattern
- Autosomal recessive
- Typical age of onset
- Infancy, Neonatal
- Estimated prevalence
- <1 / 1 000 000 (Worldwide)
- Rarity class
- <1 / 1 000 000
ORPHA:352649 is classified under "Inborn errors of metabolism" in the Orphanet nomenclature.
Common signs
- Tremor
- Hypernasal speech
- Abnormal foot morphology
- Dysdiadochokinesis
- Orofacial dyskinesia
- Sleep abnormality