Statements (34)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
neurological disorder
migraine subtype |
| gptkbp:associatedWith |
gptkb:ATP1A2
gptkb:CACNA1A gptkb:SCN1A |
| gptkbp:canBe |
familial
sporadic |
| gptkbp:cause |
confusion
genetic disorder seizures prolonged aura |
| gptkbp:diagnosedBy |
clinical evaluation
genetic testing |
| gptkbp:differentialDiagnosis |
epilepsy
stroke transient ischemic attack |
| gptkbp:firstDescribed |
1910
|
| https://www.w3.org/2000/01/rdf-schema#label |
hemiplegic migraine
|
| gptkbp:ICD-10_code |
gptkb:G43.1
|
| gptkbp:inheritance |
autosomal dominant
sporadic |
| gptkbp:onset |
childhood
adolescence |
| gptkbp:prevalence |
rare
|
| gptkbp:riskFactor |
family history of migraine
|
| gptkbp:symptom |
headache
speech difficulties sensory aura unilateral weakness visual aura |
| gptkbp:treatment |
acute migraine therapy
preventive medication |
| gptkbp:bfsParent |
gptkb:triptans
|
| gptkbp:bfsLayer |
7
|