KCNN2 Mutation in Pediatric Tremor Myoclonus Dystonia Syndrome with Electrophysiological Evaluation
Journal
Tremor and Other Hyperkinetic Movements
ISSN
2160-8288
Date Issued
2022
Author(s)
Bennett Lavenstein
Patrick McGurrin
Sanaz Attaripour
Mark Hallett
Type
Resource Types::text::journal::journal article
URL Institutional Repository
Subjects
myoclonus
;
genetics
;
physiology
;
child
;
dystonia
;
dystonic disorders
;
humans
;
male
;
movement disorders
;
mutation
;
myoclonus
;
small-conductance calcium-activated potassium channels
;
tremor
;
small conductance calcium activated potassium channel
;
kcnn2 protein, human
;
small conductance calcium activated potassium channel
;
article
;
case report
;
child
;
clinical article
;
cortical excitability
;
electrocardiography
;
electroencephalography
;
electrophysiological procedures
;
endotracheal intubation
;
extensor carpi radialis muscle
;
flexor carpi radialis muscle
;
gene
;
gene mutation
;
human
;
involuntary movement
;
kcnn2 gene
;
male
;
masseter muscle
;
mental foramen
;
motor dysfunction
;
muscle function
;
myoclonus dystonia
;
nerve stimulation
;
neurologic examination
;
nuclear magnetic resonance imaging
;
orbicularis oculi muscle
;
paraspinal muscle
;
pneumonia
;
school child
;
sensorimotor cortex
;
somatosensory evoked potential
;
sternocleidomastoid muscle
;
tandem gait test
;
tremor
;
whole exome sequencing
;
complication
;
dystonia
;
dystonic disorder
;
genetics
;
motor dysfunction
;
mutation
;
myoclonus
;
tremor