ORPHA:2131
Alternating hemiplegia of childhood
Also called AHC
- Body system
- Neurological diseases
- Inheritance pattern
- Autosomal dominant, Not applicable
- Typical age of onset
- Infancy, Neonatal
- Estimated prevalence
- 1-9 / 1 000 000 (Denmark)
- Rarity class
- 1-9 / 1 000 000
ORPHA:2131 is classified under "Neurological diseases" in the Orphanet nomenclature.
Common signs
- Gastrointestinal dysmotility
- Abnormality of the gastrointestinal tract
- Episodic hemiplegia
- Esotropia
- Exotropia
- Nystagmus