ÇOCUKLUK ÇAĞI OKSİPİTAL EPİLEPSİ: 19 HASTANIN KLİNİK DEĞERLENDİRİLMESİ
نویسندگان
چکیده
OBJECTIVE: Childhood occipital epilepsy (COE) can mainly be divided into idiopathic (IOLE) or symptomatic lobe (SOLE). Idiopathic consists of Panayiotopoulos (PS) and Gastaut syndromes (GS). In this study, we aimed to classify COE investigate the segregations between groups according clinical features.MATERIAL AND METHODS: Nineteen patients with were enrolled. Medical records evaluated. Demographic data, ictal symptoms, neurological examination, brain magnetic resonance imaging (MRI) electroencephalography (EEG) findings, family history, febrile seizure, treatment response analyzed.RESULTS: There 6 diagnosed 13 SOLE. Compared SOLE, all IOLE had a normal examination MRI findings (p=0.044 p=0.009). The most frequent symptom was generalized seizures in (100% IOLE, 75% SOLE). However, vomiting autonomic seizure PS (2/6, 2/4; 33%, 50%). Nocturnal observed more frequently than SOLE (1/13, 3/6; 8%, rate history (1 patient, 25%) found only group. Psychomotor/mental retardation common (8/13, 2/6; 62%, 33%). According outcomes, controlled one antiepileptic drug (AED) two AEDs GS. On other hand, 38% treated three AEDs.CONCLUSIONS: Normal neurologic neuroimaging are substantial features due discrimination Ictal is remarkable PS. Although psychomotor/mental higher should followed up carefully. has better outcomes
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ژورنال
عنوان ژورنال: Kocatepe T?p Dergisi
سال: 2021
ISSN: ['1302-4612']
DOI: https://doi.org/10.18229/kocatepetip.716277