International Journal of Clinical Pediatrics, ISSN 1927-1255 print, 1927-1263 online, Open Access
Article copyright, the authors; Journal compilation copyright, Int J Clin Pediatr and Elmer Press Inc
Journal website http://www.theijcp.org

Original Article

Volume 8, Number 2, October 2019, pages 32-36


Profile of Childhood Epilepsies and Syndromes Seen in an Electrophysiology Laboratory in Southeast Nigeria

Tables

Table 1. Age Distribution of Study Population
 
Age of respondents (groups)Frequency (n = 97)Percent (%)
< 1 year1111.3
1 - < 5 years3637.1
5 - < 10 years3030.9
10 - < 15 years1717.5
15 - < 18 years33.1

 

Table 2. Salient Clinical Features in the Study Population
 
Clinical/physical finding*Frequency (n = 97)Percent (%)
*Multiple responses encouraged. CT: computed tomography; MRI: magnetic resonance imaging.
Family history of seizures6567
Anti-epileptic drug therapy4647.4
Co-morbidity (at least once)2727.8
Developmental delay2525.8
Severe birth asphyxia2222.7
Microcephaly1414.4
Neuroimaging (CT/MRI)1212.4
Neonatal seizures1111.3
Poor school performance1111.3
Previous history of meningitis77.2
Developmental regression55.2
Macrocephaly55.2
Preterm delivery44.1
Head trauma with impact seizures44.1
Post term delivery11.0

 

Table 3. Spectrum of Epilepsy Types and Syndromes in the Patients
 
Epilepsy type/syndromeFrequency (n = 97)Percent (%)
Focal epilepsy3030.9
Generalized epilepsy2020.6
Benign rolandic epilepsy (BRE)1414.4
West syndrome1111.3
Combined generalized and focal epilepsy44.1
Panayiotopoulos syndrome (PS)44.1
Childhood absence epilepsy (CAE)33.1
Watanabe-Vigevano syndrome22.1
Generalized epilepsy with febrile seizure plus (GEFS+)11.0
Idiopathic generalized epilepsy with GTCSs only11.0
Juvenile myoclonic epilepsy (Janz syndrome)11.0
Lennox Gastaut syndrome (LGS)11.0
Unknown55.2

 

Table 4. Etiology of Epilepsy
 
EtiologyFrequency (n = 97)Percent (%)
Genetic4849.5
Infectious11.0
Structural44.1
Unknown/multiple4445.4