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Paroxysmal kinesigenic dyskinesia
2 OMIM references -
1 associated gene
5 connected diseases
No signs/symptoms info
Disease Type of connection
Benign familial infantile seizures
Familial or sporadic hemiplegic migraine
Infantile convulsions and choreoathetosis
Paroxysmal exertion-induced dyskinesia
Paroxysmal non-kinesigenic dyskinesia
Synonym(s):
- Familial PKD
- Familial paroxysmal kinesigenic dyskinesia
- Paroxysmal kinesigenic choreathetosis
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Diseases of the nervous system -
Epidemiological data:
Class of prevalence: 1-9 / 1 000 000
Average age onset: variable
Average age of death: normal
Type of inheritance: autosomal dominant
External references:
2 OMIM references -
No MeSH references
Gene symbol UniProt reference OMIM reference
PRRT2 Q7Z6L0614386
No signs/symptoms info available.