Difference between revisions of "Angelman syndrome"
From EEGpedia
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* Genetic disorder, loss of function in UBE3A gene on chromosome 15. | * Genetic disorder, loss of function in UBE3A gene on chromosome 15. | ||
* Clinical features apparent after birth, usually within age of 1 or 2 years old. | * Clinical features apparent after birth, usually within age of 1 or 2 years old. | ||
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==Clinics== | ==Clinics== | ||
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* Occipital discharges can be triggered by closing th eyes. | * Occipital discharges can be triggered by closing th eyes. | ||
* EEG similar in patients wit hand without seizures. | * EEG similar in patients wit hand without seizures. | ||
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Revision as of 20:30, 13 July 2017
Background
- In 1/12,000- 1/25,000 children.
- Genetic disorder, loss of function in UBE3A gene on chromosome 15.
- Clinical features apparent after birth, usually within age of 1 or 2 years old.
Clinics
- Delayed psychomotor development.
- In early years often smiling: ‘Happy puppet syndrome’.
- Overeating.
- Sleep disturbances.
- Microcephaly, large tongue and hypersalivation.
- 90% of the paients have seizures ; usually tonic or atone seizures, or absences.
- Vulnerable to infections.
EEG
- Frontal slowing
- Rhytmic discharges in 2-4Hz predominently in the frontal and/or occipital regions.
- Occipital discharges can be triggered by closing th eyes.
- EEG similar in patients wit hand without seizures.
Angelman syndrome in an 8-year-old girl (source) with frontal slowing together with occipital and frontal spikes and slow wave complexes, not synchrone
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