Periodic paralysis

GPTKB entity

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