Loading...
Publication
Neuropsychological Abnormalities in Children with the Panayiotopoulos Syndrome Point to Parietal Lobe Dysfunction
| Name: | Description: | Size: | Format: | |
|---|---|---|---|---|
| 239.3 KB | Adobe PDF |
Advisor(s)
Abstract(s)
Panayiotopoulos syndrome (PS) is a common epilepsy syndrome associated with rare clinical seizures and unknown
localization of the epileptogenic area. Despite findings of normal development in patientswith PS, recent neuropsychological studies point to subtle and diverse cognitive impairments. No well-outlined hypothesis about the localization of the brain dysfunction responsible for these impairments has been proposed.We further
explored the cognitive dysfunctions in PS andmade inferences on the most likely anatomical localization of brain
impairment. A group of 19 patients (aged 6–12) with PS was rated according to spike activity and lateralization.
The patients were submitted to a neuropsychological evaluation to assess general intelligence, memory, language,
visual–perceptual abilities, attention, and executive functions. Using 35-channel scalp EEG recordings, the N170 face-evoked event-related potential (ERP)was obtained to assess the functional integrity of the ventral pathway. All patientswith PS showed normal IQ but subtle and consistent neurocognitive impairments. Namely,
we found abnormalities in the copy task of the Rey–Osterrieth Complex Figure and in theNarrative Memory Test.
There was no correlation between neuropsychological impairments with spike activity and hemispheric spike
lateralization. The N170 ERP was normal in all patients except for one. Our neuropsychological findings demonstrate
impairments in visual–perceptual abilities and in semantic processing. These findings, paired with the absence of occipital lobe dysfunction in all neuropsychological studies of PS performed to this date, support the existence of parietal lobe dysfunction.
Description
Keywords
Epilepsia Lobo Parietal Eletroencefalografia Neuropsicologia Criança HDE NEU PED
Citation
Epilepsy Behav. 2014; 3: 50–55