ODCs

Click node...

2 OMIM references -
1 associated gene
No signs/symptoms info

COMMON GENES: 1

4 OMIM references -
4 associated genes
9 signs/symptoms

Paroxysmal kinesigenic dyskinesia

Familial or sporadic hemiplegic migraine

Citations in the biomedical literature:

Paroxysmal kinesigenic dyskinesia		Familial or sporadic hemiplegic migraine
	Synonym(s): - Familial PKD - Familial paroxysmal kinesigenic dyskinesia - Paroxysmal kinesigenic choreathetosis		Synonym(s): (no synonyms)

	Classification (Orphanet): - Rare genetic disease - Rare neurologic disease		Classification (Orphanet): - Rare genetic disease - Rare neurologic disease

	Classification (ICD10): - Diseases of the nervous system -		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		Epidemiological data: Class of prevalence: 1-5 / 10 000 Average age onset: childhood Average age of death: normal Type of inheritance: autosomal dominant

	External references: 2 OMIM references - No MeSH references		External references: 4 OMIM references - No MeSH references

Familial or sporadic hemiplegic migraine
	Very frequent - Autosomal dominant inheritance - Hemiplegia / diplegia / hemiparesia / limb palsy - Movement disorder Frequent - Ataxia / incoordination / trouble of the equilibrium - Nystagmus Occasional - EEG anomalies - Retinitis pigmentosa / retinal pigmentary changes - Sensorineural deafness / hearing loss - Speech troubles / aphasia / dysphasia / echolalia / mutism / logorrhea / dysprosodia
Paroxysmal kinesigenic dyskinesia
(no data available)