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Sleep-related hypermotor epilepsy (disorder)
Sleep-related hypermotor epilepsy
Sleep-related hyperkinetic epilepsy
SHE - sleep-related hypermotor epilepsy
A type of frontal lobe epilepsy that presents with clusters of motor seizures occurring from sleep, with usual onset in the first two decades of life, typically in adolescence (eleven to fourteen years). Focal motor seizures have hyperkinetic features or asymmetric tonic/dystonic features, usually with autonomic signs, vocalization, and negative emotional expression such as fear. Seizures are brief, with abrupt onset/offset, and there is often preserved awareness during the seizure. Individuals may describe a focal aware sensory or cognitive seizure before the motor features commence. Focal to bilateral tonic-clonic seizures can occur. Development and cognition are typically normal. Neurological examination is normal. The electroencephalogram (EEG) background is typically normal. The awake EEG is non epileptiform in most patients. During sleep, interictal epileptiform abnormalities can be seen over the frontal areas. Neuroimaging is usually normal.
Id1332160004
StatusPrimitive
SNOMED CT to ICD-10 extended map
TargetG40.1
RuleTRUE
AdviceALWAYS G40.1
CorrelationSNOMED CT source code to target map code correlation not specified
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