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dc.contributor.authorÇavuşoğlu, Dilek
dc.date.accessioned2022-04-29T12:28:54Z
dc.date.available2022-04-29T12:28:54Z
dc.date.issued2021en_US
dc.identifier.citationÇavuşoğlu, D. (2021). CHILDHOOD OCCIPITAL EPILEPSY: Childhood occipital epilepsy: clinical evaluation of 19 patients. Kocatepe Tıp Dergisi , CİLT: 22 SAYI: 3 MAYIS 2021 ÖZEL SAYISI , 168-172 . DOI: 10.18229/kocatepetip.716277en_US
dc.identifier.issn2149-7869
dc.identifier.urihttps://doi.org/10.18229/kocatepetip.716277
dc.identifier.urihttps://hdl.handle.net/20.500.12933/882
dc.description.abstractOBJECTIVE: Childhood occipital epilepsy (COE) can mainly be divided into idiopathic (IOLE) or symptomatic occipital lobe epilepsy (SOLE). Idiopathic occipital lobe epilepsy consists of Panayiotopoulos (PS) and Gastaut syndromes (GS). In this study, we aimed to classify COE and investigate the segregations between the groups according to clinical features. MATERIAL AND METHODS: Nineteen patients with COE were enrolled. Medical records of the patients were evaluated. Demographic data, ictal symptoms, neurological examination, brain magnetic resonance imaging (MRI) and electroencephalography (EEG) findings, family history, febrile seizure, and treatment response were analyzed. RESULTS: There were 6 patients diagnosed with idiopathic occipital lobe epilepsy and 13 patients diagnosed with SOLE. Compared to the SOLE, all patients of the IOLE had a normal neurological examination and MRI findings (p=0.044 and p=0.009). The most frequent ictal symptom was generalized seizures in all groups (100% IOLE, 75% SOLE). However, ictal vomiting was the most frequent autonomic seizure in IOLE and PS (2/6, 2/4; 33%, 50%). Nocturnal seizures were observed more frequently in IOLE than SOLE (1/13, 3/6; 8%, 50%). The rate of family history (1 patient, 25%) and febrile seizures (1 patient, 25%) were found in only PS group. Psychomotor/mental retardation was more common in SOLE than IOLE (8/13, 2/6; 62%, 33%). According to treatment outcomes, the seizures were controlled with one antiepileptic drug (AED) in all patients of PS and two AEDs in all patients of GS. On the other hand, 38% of patients in SOLE were treated with three or more AEDs. CONCLUSIONS: Normal neurologic examination and neuroimaging are substantial features due to discrimination between IOLE and SOLE. Ictal vomiting is a remarkable autonomic seizure in IOLE and PS. Although psychomotor/mental retardation is observed higher in SOLE than IOLE, the patients of COE should be followed up carefully. IOLE has better treatment outcomes than SOLE and PS has better than GS.en_US
dc.language.isoengen_US
dc.publisherAfyonkarahisar Sağlık Bilimleri Üniversitesien_US
dc.relation.isversionof10.18229/kocatepetip.716277en_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectOccipital epilepsyen_US
dc.subjectChilden_US
dc.subjectPanayiotopoulosen_US
dc.titleÇOCUKLUK ÇAĞI OKSİPİTAL EPİLEPSİ: 19 HASTANIN KLİNİK DEĞERLENDİRİLMESİen_US
dc.title.alternativeCHILDHOOD OCCIPITAL EPILEPSY: CLINICAL EVALUATION OF 19 PATIENTS
dc.typearticleen_US
dc.authorid0000-0003-4924-5300en_US
dc.departmentAFSÜ, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü, Çocuk Sağlığı ve Hastalıkları Ana Bilim Dalıen_US
dc.contributor.institutionauthorÇavuşoğlu, Dilek
dc.identifier.volume22en_US
dc.identifier.issue3en_US
dc.identifier.startpage168en_US
dc.identifier.endpage172en_US
dc.relation.journalKocatepe Tıp Dergisien_US
dc.relation.publicationcategoryMakale - Ulusal Hakemli Dergi - Kurum Öğretim Elemanıen_US


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