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Journal articles on the topic 'Child with epilepsy'

Author: Grafiati

Published: 4 June 2021

Last updated: 13 February 2022

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1

Trescher, WilliamH. "Your child and epilepsy." Electroencephalography and Clinical Neurophysiology 103, no. 2 (1997): 331–32. http://dx.doi.org/10.1016/s0013-4694(96)96928-x.

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2

Vining, Eileen P. G. "Will My Child Grow up and be Normal?" Epilepsy Currents 5, no. 4 (2005): 155–56. http://dx.doi.org/10.1111/j.1535-7511.2005.00046.x.

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Physical Growth and Endocrinal Disorders during Pubertal Maturation in Girls with Epilepsy El-Khayat HA, Abd El-Basset FZ, Tomoum HY, Tohamy SM, Zaky AA, Mohamed MS, Hakky SM, Barbary NS, Nassef NM Epilepsia 2004;45:1106–1115 Purpose This study investigated the effect of epilepsy or antiepileptic drugs or both on the physical growth, pubertal development, and androgenic status of girls with epilepsy between ages 8 and 18 years. Methods Sixty-six female patients with epilepsy, their mean ages 13.47 ± 3.5 years, were included. Anthropometric measurements, staging of pubertal maturation, and clin

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3

Bernier, A., JS Landry, AS Kristof, L. Carmant, and P. Major. "Child Neurology (General Pediatric Neurology)." Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques 42, S1 (2015): S23. http://dx.doi.org/10.1017/cjn.2015.117.

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Background: Tuberous sclerosis complex (TSC) is a neurocutaneous syndrome that can present with many disabling neurological symptoms, the most common being seizures. Although it is a chronic systemic syndrome, healthcare utilization and long-term outcome of subjects with TSC are not well defined. The goal of this study was to evaluate the direct cost and long-term outcome of TSC compared to other forms of epilepsy and healthy controls. Methods: Our provincial health care database was interrogated to determine use of medical services by patients with TSC, epilepsy and healthy controls from 1996

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4

Desmeules, M., C. Cieuta-Walti, G. Sébire, et al. "Child Neurology (Epilepsy and EEG)." Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques 42, S1 (2015): S22. http://dx.doi.org/10.1017/cjn.2015.112.

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Background: Febrile infection-related epilepsy syndrome (FIRES) is a devastating entity characterized by acute onset of refractory epileptic status preceded by a febrile infection, for which no aetiology has been identified so far. Methods: We report the cases of two males presenting with typical FIRES, for whom extensive investigations revealed no specific aetiology. Failure of controlling seizures with multiple anticonvulsants as well as barbiturate coma lead to the decision to try immunotherapy. The first patient received plasma exchange after a negative trial of IVIGs, while the second rec

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5

Kaneko, Sunao. "Epilepsy, Pregnancy, and the Child." Epilepsia 41, s9 (2000): 8–13. http://dx.doi.org/10.1111/j.1528-1157.2000.tb02211.x.

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6

Gulati, S., and L. Kumar. "'Chest epilepsy' in a child." Postgraduate Medical Journal 68, no. 799 (1992): 369–70. http://dx.doi.org/10.1136/pgmj.68.799.369.

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7

Scorza, Fulvio A., Vera C. Terra, Ricardo M. Arida, Américo C. Sakamoto, and Ronald M. Harper. "Sudden death in a child with epilepsy: potential cerebellar mechanisms?" Arquivos de Neuro-Psiquiatria 69, no. 4 (2011): 707–10. http://dx.doi.org/10.1590/s0004-282x2011000500024.

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Epilepsy is the most common neurological disorder in humans. People with epilepsy are more likely to die prematurely than those without epilepsy, with the most common epilepsy-related category of death being sudden unexpected death in epilepsy (SUDEP). The central mechanisms underlying the fatal process remain unclear, but cardiac and respiratory mechanisms appear to be involved. Recently, cerebellar, thalamic, basal ganglia and limbic brain structures have been shown to be implicated in respiratory and cardiac rate regulation. We discuss here the potential mechanisms underlying the fatal proc

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8

Aldenkamp, A. "The child with epilepsy at school." European Journal of Paediatric Neurology 12 (May 2008): S10. http://dx.doi.org/10.1016/s1090-3798(08)70033-3.

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9

Lunn, Judith, Charlie Lewis, and Emily Gannon. "Parent–child mentalizing in pediatric epilepsy." Epilepsy & Behavior 96 (July 2019): 6–12. http://dx.doi.org/10.1016/j.yebeh.2019.03.052.

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10

Millichap, J. G. "Child Perspectives on Disclosing Epilepsy Diagnosis." AAP Grand Rounds 35, no. 3 (2016): 34. http://dx.doi.org/10.1542/gr.35-3-34.

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11

Wachter, Kerri. "Psychiatric Conditions Common in Child Epilepsy." Clinical Psychiatry News 33, no. 3 (2005): 34. http://dx.doi.org/10.1016/s0270-6644(05)70042-4.

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12

Bax, Martin. "Problems for the child with epilepsy." Developmental Medicine & Child Neurology 41, no. 11 (1999): 723. http://dx.doi.org/10.1017/s0012162299001474.

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13

Kuroiwa, T., H. Morita, H. Tanabe, and T. Ohta. "Life threatening epilepsy in a child." Journal of Neurology, Neurosurgery & Psychiatry 57, no. 11 (1994): 1440–41. http://dx.doi.org/10.1136/jnnp.57.11.1440.

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14

Tenney, J. R., and M. B. Schapiro. "Child Neurology: Hemiconvulsion-hemiplegia-epilepsy syndrome." Neurology 79, no. 1 (2012): e1-e4. http://dx.doi.org/10.1212/wnl.0b013e31825dce5f.

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15

Bricklebank, Karen. "Supporting the young child with epilepsy." Practical Pre-School 2001, no. 27 (2001): 9–10. http://dx.doi.org/10.12968/prps.2001.1.27.40861.

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16

Lanfear, Judith, and Alison Fielder. "The child/young person with epilepsy." Paediatric Nursing 10, no. 3 (1998): 29–36. http://dx.doi.org/10.7748/paed.10.3.29.s22.

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17

Kraus, Donna M. "Book Review: Your Child and Epilepsy." Annals of Pharmacotherapy 32, no. 10 (1998): 1116. http://dx.doi.org/10.1177/106002809803201004.

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18

Sun, Ying, Xuehua Shen, Qiubo Li, and Qingxia Kong. "Child with cerebral malformations and epilepsy." International Journal of Neuroscience 128, no. 9 (2018): 881–85. http://dx.doi.org/10.1080/00207454.2018.1433177.

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19

Bax, Martin. "Problems for the child with epilepsy." Developmental Medicine & Child Neurology 41, no. 11 (2007): 723. http://dx.doi.org/10.1111/j.1469-8749.1999.tb00531.x.

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20

Sethi, N. K., and J. R. Tenney. "Child Neurology: Hemiconvulsion-hemiplegia-epilepsy syndrome." Neurology 79, no. 24 (2012): 2367–68. http://dx.doi.org/10.1212/01.wnl.0000424157.07211.bf.

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21

Wolf, Peter. "Epilepsy in Contemporary Fiction: Fates of Patients." Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques 27, no. 2 (2000): 166–72. http://dx.doi.org/10.1017/s0317167100052306.

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ABSTRACT:Fictional accounts of epilepsy are of interest because they may convey information on images and public views of epilepsy which are not contained in medical texts. Thus, medical and nonmedical traditions together form the cultural history of epilepsy. Of the numerous possible aspects of epilepsy in fiction, this paper looks especially at the writers'background of knowledge about epilepsy; epilepsy as a handicap and a reason for social rejection, with special reference to epilepsy under the Nazi rule; threats to patients'lives; the motive of the child with epilepsy as a divine child; a

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22

Meador, Kimford. "Valproate Poses Risk to Unborn Child." Epilepsy Currents 5, no. 3 (2005): 116–17. http://dx.doi.org/10.1111/j.1535-7511.2005.05305.x.

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The Longer Term Outcome of Children Born to Mothers with Epilepsy Adab N, Kini U, Vinten J, Ayres J, Baker G, Clayton-Smith J, Coyle H, Fryer A, Gorry J, Gregg J, Mawer G, Nicolaides P, Pickering L, Tunnicliffe L, Chadwick DW J Neurol Neurosurgsychiatry 2004;75:1575–1583 Objectives To determine the prevalence of cognitive delay and possible associated dysmorphic features in children exposed to antiepileptic drugs (AEDs) in utero. Methods In a retrospective study of children born to mothers with epilepsy, in regional epilepsy clinics in Liverpool and Manchester, U.K., the children were aged bet

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23

Vujisic, Slavica, and Sanja Vodopic. "Epilepsy awareness, knowledge and attitudes among secondary school teachers in Montenegro." Srpski arhiv za celokupno lekarstvo 145, no. 3-4 (2017): 129–35. http://dx.doi.org/10.2298/sarh160218026v.

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Introduction/Objective. Epilepsy is associated with numerous misconceptions due to its dramatic manifestation and poor knowledge among the public. The aim of this study was to assess epilepsy awareness, knowledge and attitudes among secondary school teachers. Methods. We conducted a cross-sectional survey by sending a simple self-administered questionnaire to all secondary schools in Podgorica, Montenegro. The questionnaire contained 16 questions regarding epilepsy awareness, knowledge and attitudes, first aid attitudes, as well as demographic and teaching experience data. Results. We analyzed

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24

Sari, Novi Komala, Nina Herlina, and Aswan Jhonet. "HUBUNGAN RIWAYAT KEJANG DEMAM DENGAN KEJADIAN EPILEPSI PADA ANAK ≤ 5 TAHUN DI RSUD Dr. H. ABDUL MOELOEK PROVINSI LAMPUNG TAHUN 2018-2019." Jurnal Kebidanan Malahayati 7, no. 3 (2021): 453–58. http://dx.doi.org/10.33024/jkm.v7i3.4203.

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Background : Epilepsy is a neurological disorder which often found in the world and has the highest incidence in children. The most common risk factor of epilepsy is febrile seizure. Febrile seizure refer to a seizure following by high-fever (>38°C) that often found in the age between 6 month – 5 years old. Objective : This study aim to acknowledge the relation between the febrile sizure history and the incidence of epilepsy found in the children of ≤ 5 years old in RSUD Dr. H. Abdul Moeloek Lampung Province 2018-2019. Methods: This study used an analytic research design with cross sectiona

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25

Wijaya, I. Made Ananta, Alifiani Hikmah Putranti, and Maria Mexitalia. "Ketogenic Diet for Treatment 2-Year 9 Month Old Boy With Intractable Epilepsy." Medica Hospitalia : Journal of Clinical Medicine 6, no. 2 (2019): 137–42. http://dx.doi.org/10.36408/mhjcm.v6i2.395.

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Background:The ketogenic diet (KD) is a high-fat, low-carbohydrate, and normal-protein diet that has been used for the treatment of medically refractory childhood epilepsy since the 1920s.The KD includes 80% fat, 15% protein, and 5% carbohydrate; the ratio of fat to carbohydrate plus protein ranges from 2:1 to 4:1.The purpose of the case report was to learn benefits and factors that influence the administration of the ketogenic diet in intractable epilepsy. Case:A 2-years 9 months old boy since 3 month of age the child begins seizure. Five month the child was diagnosed with epilepsy rece

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26

N, Kiseleva, and Kiselev S. "A-149 Boy with Rolandic Epilepsy Benefited from Visuospatial Training." Archives of Clinical Neuropsychology 35, no. 6 (2020): 943. http://dx.doi.org/10.1093/arclin/acaa068.149.

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Abstract Objective Children with epilepsy can have delay in the development of neurocognitive abilities. It is important to receive the evidence for efficiency of different treatments that are aimed to help children with epilepsy. The goal of this study was to assess the impact of 16 weeks of visuospatial training on the visuospatial abilities in 7 years of age child with Rolandic epilepsy. Methods The child is 7 year old boy with Rolandic epilepsy. The neuropsychological assessment of child has revealed the deficit in visuospatial abilities. Child participated in 16 weeks of visuospatial trai

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27

Hindler, C. G. "Epilepsy and Violence." British Journal of Psychiatry 155, no. 2 (1989): 246–49. http://dx.doi.org/10.1192/bjp.155.2.246.

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Epileptic automatism and violence are seldom found among temporal lobe epileptics. The case of a 19-year-old girl who killed a 20-month-old child during an epileptic attack is described, and the literature and medico-legal issues are briefly reviewed.

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28

Crozier, Denise, and Katherine Martin. "Fifteen-minute consultation: Epilepsy in the child with intellectual disabilities—aetiology." Archives of disease in childhood - Education & practice edition 105, no. 4 (2019): 204–8. http://dx.doi.org/10.1136/archdischild-2019-316975.

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Epilepsies are a relatively common group of disorders affecting children and young people. Children with intellectual disabilities have an increased risk of developing an epilepsy, and children with epilepsy are more likely to have difficulties with learning or development than those who do not have an epilepsy. Assessment in this group can be more challenging but is particularly important as it may provide information regarding a potential unifying diagnosis, prognosis and best treatment options.

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29

Millichap, J. Gordon. "Gourmand Syndrome in a Child with Epilepsy." Pediatric Neurology Briefs 22, no. 9 (2008): 70. http://dx.doi.org/10.15844/pedneurbriefs-22-9-7.

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30

Ceylaner, Gülay, Serdar Ceylaner, and Aydan Değerliyurt. "A child with XYY karyotype and epilepsy." Journal of Pediatric Neurology 09, no. 02 (2015): 255–58. http://dx.doi.org/10.3233/jpn-2011-0479.

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31

Sripathi, Rachana, and Lalitha Sivaswamy. "A Child with Epilepsy and Skin Lesions." Journal of Pediatrics 163, no. 5 (2013): 1522–1522. http://dx.doi.org/10.1016/j.jpeds.2013.05.043.

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32

Golomb, Meredith R., Anna Illner, Celanie K. Christensen, and Laurence E. Walsh. "A Child With Friedreich's Ataxia and Epilepsy." Journal of Child Neurology 20, no. 3 (2005): 248–50. http://dx.doi.org/10.1177/08830738050200031201.

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33

AUSTIN, JOAN KESSNER. "Childhood Epilepsy: Child Adaptation and Family Resources." Journal of Child and Adolescent Psychiatric Nursing 1, no. 1 (1988): 18–24. http://dx.doi.org/10.1111/j.1744-6171.1988.tb00222.x.

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34

Yang, Zhixian, Xiaoyan Liu, Xiaosong Dong, Jiong Qin, Jing Li, and Fang Han. "Epilepsy and Narcolepsy-Cataplexy in a Child." Journal of Child Neurology 27, no. 6 (2012): 807–10. http://dx.doi.org/10.1177/0883073811432888.

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35

Nakagawa, Hidenori, Shin Okazaki, Mikiko Koizumi, Marina Nishida, Naomi Ishii, and Kazuyoshi Fukai. "Bromoderma in a child with refractory epilepsy." Pediatrics International 61, no. 7 (2019): 738. http://dx.doi.org/10.1111/ped.13895.

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36

Kubiski, Rachael. "Perioperative Care of the Child With Epilepsy." AORN Journal 95, no. 5 (2012): 635–47. http://dx.doi.org/10.1016/j.aorn.2012.02.006.

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37

Plioplys, Sigita, David W. Dunn, Tatiana Falcone, and Jana E. Jones. "34.0 Update on Epilepsy for Child Psychiatrists." Journal of the American Academy of Child & Adolescent Psychiatry 56, no. 10 (2017): S50—S51. http://dx.doi.org/10.1016/j.jaac.2017.07.198.

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38

Nelson, Elizabeth, and Mariellen Fischer. "Neuropsychological Evaluation of the Child with Epilepsy." Disease-a-Month 53, no. 3 (2007): 162–68. http://dx.doi.org/10.1016/j.disamonth.2007.04.007.

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39

Mitic, Vesna, Goran Cuturilo, Ivana Novakovic, et al. "Epilepsy in a child with Wolf-Hirschhorn syndrome." Srpski arhiv za celokupno lekarstvo 139, no. 11-12 (2011): 795–99. http://dx.doi.org/10.2298/sarh1112795m.

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Introduction. Wolf-Hirschhorn syndrome (WHS) is a rare chromosomal disorder characterized by facial dismorphy, multiple congenital anomalies, delayed psychomotor development and pharmaco-resistant epilepsy. Case Outline. We present a 5-year-old girl with severe delay in growth and development, microcephaly, mild facial dismorphy and epilepsy. The pregnancy was complicated by intrauterine growth retardation. Generalized muscle hypotonia was observed at birth. First seizures started at age of 9 months as unilateral convulsive status epilepticus (SE), sometimes with bilateral generalization. Seiz

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40

Tomson, Torbjörn, Giulia Muraca, and Neda Razaz. "Paternal exposure to antiepileptic drugs and offspring outcomes: a nationwide population-based cohort study in Sweden." Journal of Neurology, Neurosurgery & Psychiatry 91, no. 9 (2020): 907–13. http://dx.doi.org/10.1136/jnnp-2020-323028.

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ObjectivesTo investigate the association between paternal use of antiepileptic drugs (AEDs) and adverse neurodevelopmental outcomes and major congenital malformations (MCM) in the offspring.MethodsUsing nationwide Swedish registries, we included 1 144 795 births to 741 726 fathers without epilepsy and 4544 births to 2955 fathers with epilepsy. Of these, 2087 (45.9%) were born to fathers with epilepsy who had dispensed an AED during the conception period. Children who had both parents with epilepsy were excluded. The incidence rate of MCM, autism spectrum disorder, attention deficit hyperactivi

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41

Lothman, Deborah J., Robert C. Pianta, and Sheila M. Clarson. "Mother-child interaction in children with epilepsy: Relations with child competence." Journal of Epilepsy 3, no. 3 (1990): 157–63. http://dx.doi.org/10.1016/0896-6974(90)90102-5.

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42

Wirrell, Elaine C., Zachary M. Grinspan, Kelly G. Knupp, et al. "Care Delivery for Children With Epilepsy During the COVID-19 Pandemic: An International Survey of Clinicians." Journal of Child Neurology 35, no. 13 (2020): 924–33. http://dx.doi.org/10.1177/0883073820940189.

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Objective: To evaluate the effect of the COVID-19 pandemic on global access to care and practice patterns for children with epilepsy. Methods: We conducted a cross-sectional, online survey of pediatric neurologists across the world affiliated with the International Child Neurology Association, the Chinese Child Neurology Society, the Child Neurology Society, and the Pediatric Epilepsy Research Consortium. Results were analyzed in relation to regional burden of COVID-19 disease. Results: From April 10 to 24, 2020, a sample of 212 respondents from 49 countries indicated that the COVID-19 pandemi

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43

Subakti, Charles, Madarina Julia, and Agung Triono. "Duration of active epilepsy as a predictor of seizure control after relapse in child epilepsy." Paediatrica Indonesiana 60, no. 4 (2020): 202–7. http://dx.doi.org/10.14238/pi60.4.2020.202-7.

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Background Epilepsy is a chronic illness that may affect childhood growth and development. Some epilepsy cases are easy to control, either with monotherapy or politherapy antiepilepticdrugs, but many cases are difficult to control. Several factors influence the risk of relapse, but information is limited on factors predictive of seizure control after relapse. Our study investigate patient with epilepsy relaps and see whether the duration of active epilepsy prior to initial remission can be use as a predictor of seizure control after relaps. Objective To assess whether duration of active

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44

Jayaram, Shoba, Modhi Alkhaldi, and Asim Shahid. "The Role and Controversies of Electroencephalogram in Focal versus Generalized Epilepsy." Journal of Pediatric Epilepsy 10, no. 02 (2021): 058–64. http://dx.doi.org/10.1055/s-0041-1722869.

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AbstractAs early in 1935, Gibbs et al described electroencephalogram (EEG) features of large slow waves seen in “petit mal” seizures and change in background rhythm to a higher frequency, greater amplitude pattern in “grand mal” seizures. Studies have shown many typical EEG features in focal onset as well as generalized epilepsies.2 3 It is usually easy to delineate focal epilepsy cases when EEG onset of seizures is clear as seen in Benign focal epileptiform discharges of childhood.4 However, it is not uncommon to see cases where epileptiform discharges are not very clear. For example, there c

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45

O'Toole, Stephanie, Veronica Lambert, Pamela Gallagher, Amre Shahwan, and Joan K. Austin. "Talking about epilepsy: Challenges parents face when communicating with their child about epilepsy and epilepsy-related issues." Epilepsy & Behavior 57 (April 2016): 9–15. http://dx.doi.org/10.1016/j.yebeh.2016.01.013.

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46

Liu, Yin, David Michelson, Robin Clark, and June-Anne Gold. "Child Neurology: Siblings with infantile epilepsy and developmental delay." Neurology 91, no. 3 (2018): 143–47. http://dx.doi.org/10.1212/wnl.0000000000005815.

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ObjectiveChromosome 14q11-q22 deletion syndrome (OMIM 613457) is a rare genomic disorder with a variable phenotype.MethodsWe report 2 full siblings, a brother and sister, with a unique familial 2.4 Mb microdeletion at 14q13.1–14q13.3 by microarray (first identified in the brother, Mayo Clinical Laboratories, 2010).ResultsBoth children presented with infantile spasms that evolved to intractable epilepsy and profound developmental delay. They share distinctive dysmorphic features: long expressionless facies, full cheeks, flattened midface, full lips, and generalized hypotonia. Only the sister ha

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47

Subki, Ahmed Hussein, Abdel Moniem Mukhtar, Rakan Salah Al-Harbi, et al. "The Impact of Pediatric Epilepsy on Children and Families: A Multicenter Cross-Sectional Study." Clinical Practice & Epidemiology in Mental Health 14, no. 1 (2018): 323–33. http://dx.doi.org/10.2174/1745017901814010323.

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Background and Objectives: Epilepsy is considered one of the most prevalent causes of morbidity in children. The aim of this study is to determine how epilepsy impacts the lives of children with epilepsy and their families. Methods: A translated version of the “Impact of Pediatric Epilepsy Scale” (IPES) questionnaire was completed by the 80 mothers of children with epilepsy, recruited at three hospitals in Jeddah, Saudi Arabia This is a validated self-administered questionnaire used to assess the impact of epilepsy on the lives of the child and family, as well as the quality of life (QoL) of t

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48

Szczepanik, E., and I. Terczyńska. "The coexistence of idiopathic partial epilepsy and idiopathic generalized epilepsy in one child." European Journal of Paediatric Neurology 12 (May 2008): S35. http://dx.doi.org/10.1016/s1090-3798(08)70114-4.

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49

Harijan, Pooja, Arnab Kumar Seal, Manish Prasad, and William P. Whitehouse. "Fifteen-minute consultation: When medicines don’t work—the child with poorly controlled seizures." Archives of disease in childhood - Education & practice edition 104, no. 3 (2018): 135–40. http://dx.doi.org/10.1136/archdischild-2018-316035.

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Drug-resistant epilepsy (DRE) occurs in 20%–30% of children with epilepsy with significant impact on their quality of life. Management of this group of children has greatly improved in the recent years with streamlining of epilepsy surgery services and associated quaternary multimodal evaluation. This article provides a review of DRE in children and management based on recent evidence and published opinion. We have also presented an algorithmic approach to the child with possible DRE.

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50

N, Kiseleva, and Kiselev S. "A-150 Motor Sequencing Training Improved Executive Abilities in a Boy with Rolandic Epilepsy." Archives of Clinical Neuropsychology 35, no. 6 (2020): 944. http://dx.doi.org/10.1093/arclin/acaa068.150.

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Abstract Objective It is known that children with epilepsy can have deficit in neurocognitive abilities. It is of great significance to receive the evidence for efficiency of different treatments that are aimed to help children with epilepsy. The goal of this study was to reveal the impact of 12 weeks of motor sequencing training on the executive abilities in a child with Rolandic epilepsy. Methods The child is 7 year old boy. The neuropsychological assessment of child has revealed the mild deficit in executive abilities. Child participated in 12 weeks of motor sequencing training. A total of

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