Early-onset epilepsy in infancy exhibits heterogeneous features and the ILAE framework facilitates a systematic diagnostic approach and supports clinical management in pediatric patients.
Early diagnosis, comprehensive treatment with appropriate antiepileptic drug selection based on seizure type and epilepsy etiology, and rehabilitation improve prognosis and quality of life for children with epilepsy.
L. B. Novikova, K. M. Ziultsle, A. Akopyan et al.· Epilepsy and paroxysmal cond...· 0 citations
The relationship between electroclinical features and etiology, as well as the genotype-phenotype characterizations and prognosis with genetically determined DEEs, are defined and several novel variants in disease-associated genes are described.
Burcu Yaman, F. Kurekci, Sinan Akbaş et al.· Epileptic disorders· 0 citations
Generalized seizures with tonic clonic presentation were most common seizure type reported and were classified according to International League Against Epilepsy classification 1989.
Critical unmet needs include earlier molecular diagnosis, precision therapies targeting developmental outcomes beyond seizure control, and prospective international registries to characterize the long-term natural history of EIDEE.
Debopam Samanta· Brain & development (Tokyo....· 0 citations
Epileptic seizures in patients with KBG syndrome are usually generalized and have an onset between infancy and mid-teens, and common epileptological features in KBG syndrome comprise the good response to antiseizure medication and, in most cases, the remitting nature of epilepsy.
S. Kalampokini, Evripidis Pityrigkas, Zoi Kallia et al.· Epileptic disorders· 0 citations
Children with NF1 and IESS commonly present with the typical triad of IESS, and some patients show NF1-related T2 hyperintense lesions in the basal ganglia on brain magnetic resonance imaging.
Lian-Yue Wang, Zhan-Wei Zhang, Z. Pan et al.· Zhongguo dang dai er ke za z...· 0 citations
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