Idiopathic generalized epilepsy in adults - Daoud, Sawsan;Farhat, Nouha;Damak, Mariem
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Idiopathic epilepsy (IE) accounts for 20% of all epilepsies, but less than 1% of research into this disease. This imbalance reflects a lack of awareness of the diagnostic difficulties, especially in cases of late onset or atypical signs.We conducted a retrospective study including adults followed for AR. We identified the distinctive clinical and paraclinical criteria of the different syndromes in adults.EI-CGTC was the most frequent epileptic syndrome (78.7%), followed by EMJ (17.32%). Family history of epilepsy and clinical photosensitivity were more frequent in EMJ…mehr

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Produktbeschreibung
Idiopathic epilepsy (IE) accounts for 20% of all epilepsies, but less than 1% of research into this disease. This imbalance reflects a lack of awareness of the diagnostic difficulties, especially in cases of late onset or atypical signs.We conducted a retrospective study including adults followed for AR. We identified the distinctive clinical and paraclinical criteria of the different syndromes in adults.EI-CGTC was the most frequent epileptic syndrome (78.7%), followed by EMJ (17.32%). Family history of epilepsy and clinical photosensitivity were more frequent in EMJ (p=0.01).Electroencephalographically, generalized intercritical abnormalities, photo-paroxysmal response and HPN-triggered electrical abnormalities were predominantly recorded during EMJ (p = 0.000, p < 0.05 and 0.001 respectively). Focal abnormalities were recorded during these 2 syndromes. Knowledge of the characteristics of AR syndromes could improve patient management and better guide subsequent epidemiological and genetic studies.
Autorenporträt
Sawsan DAOUD BEN SALAH: Assistente do Hospital Universitário, Departamento de Neurologia, CHU Habib Bourguiba Sfax, Tunísia. Diploma em epileptologia, diploma em patologia neurovascular, diploma em educação médica básica, mestrado em pesquisa em neurociência.