Statements (47)
Predicate | Object |
---|---|
gptkbp:instanceOf |
gptkb:disease
muscular dystrophy |
gptkbp:affects |
gptkb:skeletal_muscle
muscle function |
gptkbp:associatedWith |
gptkb:KCNJ2
CACNA1S SCN4A ion channel dysfunction |
gptkbp:canBe |
episodic
familial sporadic |
gptkbp:cause |
respiratory muscle weakness
|
gptkbp:characterizedBy |
episodes of muscle paralysis
episodes of muscle weakness |
gptkbp:diagnosedBy |
clinical evaluation
genetic testing electromyography serum potassium measurement |
gptkbp:firstDescribed |
19th century
|
gptkbp:gender |
affects both males and females
|
https://www.w3.org/2000/01/rdf-schema#label |
Periodic paralysis
|
gptkbp:ICD-10_code |
G72.3
|
gptkbp:inheritance |
true
|
gptkbp:MeSH_ID |
D010522
|
gptkbp:obtainedFrom |
true
|
gptkbp:OMIM |
168300
|
gptkbp:onset |
childhood
adolescence |
gptkbp:prevalence |
rare
|
gptkbp:subspecies |
gptkb:Andersen-Tawil_syndrome
hyperkalemic periodic paralysis hypokalemic periodic paralysis paramyotonia congenita |
gptkbp:symptom |
muscle stiffness
muscle weakness muscle paralysis |
gptkbp:treatment |
avoiding triggers
potassium supplements carbonic anhydrase inhibitors dietary modifications |
gptkbp:triggeredBy |
cold
stress exercise high carbohydrate meals rest after exercise |
gptkbp:bfsParent |
gptkb:LQT7
|
gptkbp:bfsLayer |
7
|