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autosomaal dominante nachtelijke frontalekwabepilepsie (aandoening)
autosomaal dominante nachtelijke frontalekwabepilepsie
autosomaal dominante nachtelijke frontale epilepsie
ADNFLE
Familial sleep-related hypermotor epilepsy
Autosomal dominant nocturnal frontal lobe epilepsy
ADNFLE - Autosomal dominant nocturnal frontal lobe epilepsy
ADSHE - Autosomal dominant sleep-related hypermotor epilepsy
Autosomal dominant sleep-related hypermotor epilepsy
Autosomal dominant sleep-related hyperkinetic epilepsy
A type of familial frontal lobe epilepsy where individuals present 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. 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 are seen over the frontal areas in approximately 50% of patients. Neuroimaging is usually normal. There is a family history of sleep-related hypermotor epilepsy.
Id698021005
StatusPrimitive
DHD Diagnosis thesaurus reference set
RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set
TargetG40.2
TermLokalisatiegebonden (focale)(partiƫle) symptomatische epilepsie en epileptische syndromen met complexe partiƫle aanvallen
SNOMED CT to Orphanet simple map98784
SNOMED CT to ICD-10 extended map
TargetG40.1
RuleTRUE
AdviceALWAYS G40.1
CorrelationSNOMED CT source code to target map code correlation not specified