ORPHA:569
Familial or sporadic hemiplegic migraine
- Body system
- Neurological diseases
- Inheritance pattern
- Autosomal dominant
- Typical age of onset
- Childhood
- Estimated prevalence
- 1-5 / 10 000 (Europe)
- Rarity class
- 1-5 / 10 000
ORPHA:569 is classified under "Neurological diseases" in the Orphanet nomenclature.
Common signs
- Muscle weakness
- Migraine with aura
- Abnormality of speech or vocalization
- EEG abnormality
- Focal motor seizure
- Focal sensory seizure