Literature DB >> 19339285

Clinical and EEG features of epilepsy in children and adolescents in Down syndrome.

Joanna Smigielska-Kuzia1, Wojciech Sobaniec, Wojciech Kułak, Leszek Boćkowski.   

Abstract

Epilepsy is rarely considered as a major component of Down syndrome. We evaluated the prevalence of epileptic seizures in 252 (97 girls and 155 boys) children and adolescents with Down syndrome evaluated at Department of Pediatric Neurology between 1994 and 2007. Results showed that 15 (6%) patients had epileptic seizures: 8 partial seizures; 1 infantile spasms, 1 Lennox-Gastaut syndrome, and 5 generalized tonic-clonic seizures. Electroencephalography was performed on all patients with Down syndrome. Focal changes, spikes, generalized slowing, and hypsarrhythmia were recorded. The electroencephalography was found to be abnormal in Down syndrome with epilepsy in 100%. Almost 60% of patients with Down syndrome and epilepsy had seizures, but 40% of the patients were seizures-free. Quantitative electroencephalography analysis revealed significant differences between children with Down syndrome and the control groups in the alpha, delta, and beta rhythms. Our findings are in accordance with other reports.

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Year:  2009        PMID: 19339285     DOI: 10.1177/0883073808324542

Source DB:  PubMed          Journal:  J Child Neurol        ISSN: 0883-0738            Impact factor:   1.987


  8 in total

Review 1.  Epilepsy genetics--past, present, and future.

Authors:  Annapurna Poduri; Daniel Lowenstein
Journal:  Curr Opin Genet Dev       Date:  2011-01-27       Impact factor: 5.578

2.  Down Syndrome iPSC-Derived Astrocytes Impair Neuronal Synaptogenesis and the mTOR Pathway In Vitro.

Authors:  Bruno H S Araujo; Carolini Kaid; Janaina S De Souza; Sérgio Gomes da Silva; Ernesto Goulart; Luiz C J Caires; Camila M Musso; Laila B Torres; Adriano Ferrasa; Roberto Herai; Mayana Zatz; Oswaldo K Okamoto; Esper A Cavalheiro
Journal:  Mol Neurobiol       Date:  2017-11-11       Impact factor: 5.590

3.  Intellectual disability and epilepsy in down syndrome.

Authors:  Diana Barca; Oana Tarta-Arsene; Alice Dica; Catrinel Iliescu; Magdalena Budisteanu; Cristina Motoescu; Niculina Butoianu; Dana Craiu
Journal:  Maedica (Buchar)       Date:  2014-12

Review 4.  Neurological phenotypes for Down syndrome across the life span.

Authors:  Ira T Lott
Journal:  Prog Brain Res       Date:  2012       Impact factor: 2.453

Review 5.  Neurologic complications of Down syndrome: a systematic review.

Authors:  Jonathan D Santoro; Dania Pagarkar; Duong T Chu; Mattia Rosso; Kelli C Paulsen; Pat Levitt; Michael S Rafii
Journal:  J Neurol       Date:  2020-09-12       Impact factor: 6.682

6.  Neurodevelopmental outcomes in children with Down syndrome and infantile spasms.

Authors:  Sarah Tapp; Tovi Anderson; Jeannie Visootsak
Journal:  J Pediatr Neurol       Date:  2015-06

7.  Implications of delayed diagnosis of infantile spasm in a child with Down syndrome.

Authors:  Allison Buterbaugh; Jeannie Visootsak
Journal:  J Pediatr Neurol       Date:  2014

8.  Down syndrome and the molecular pathogenesis resulting from trisomy of human chromosome 21.

Authors:  Aarti Ruparelia; Frances Wiseman; Olivia Sheppard; Victor L J Tybulewicz; Elizabeth M C Fisher
Journal:  J Biomed Res       Date:  2010-03
  8 in total

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