Childhood epilepsy

Authors

  • Sueli Rizzutti Médica Neuropediatra e Mestre em Neurologia pela Escola Paulista de Medicina – Unifesp.
  • Mauro Muszkat Médico Neuropediatra e Doutor em Neurologia pela Escola Paulista de Medicina – Unifesp.
  • Luiz Celso Pereira Vilanova Professor-adjunto Doutor e Chefe do Setor de Neurologia Infantil da Disciplina de Neurologia da Escola Paulista de Medicina – Unifesp

DOI:

https://doi.org/10.34024/rnc.2000.v8.8939

Keywords:

Epilepsia na infância, síndromes epilépticas

Abstract

Epileptic seizures represent one of the most frequently occurring neurologic disorders in children. Between 0,5% and 1% of children and adolescents experience seizures associated with other acute metabolic or neurologic insults; most of them occur in the neonatal period. The highest incidence of epilepsy is in the first year of life. West syndrome accounts for about 9% of all childhood epilepsy, Lennox-Gastaut syndrome for 1% to 2%, childhood absence epilepsy for 10% to 15% and juvenile myoclonic epilepsy for 5%. Idiopathic localization-related epilepsy (benign rolandic epilepsy and its variants) may account for 10% of all childhood epilepsy but 20% to 25% of epilepsy are diagnosed between the ages of 5 and 15 years.

Metrics

Metrics Loading ...

References

Volpe JJ. Neonatal Seizures (Chapter 5). In: Volpe JJ. Neurology of the Newborn, Philadelphia, WB Saunders Co, 1981.

Volpe JJ. Neonatal Seizures. Clin Perinatology, 4:43, 1977.

Kuzniecky R, Murro A, King D. Magnetic resonance imaging in childhood intractable partial epilepsies: pathologic correlations. Neurology, 43:681-7, 1993.

Plouin P. Benign idiopathic neonatal convulsions (familial and non-familial). In: Roger P, Bureau M, Dravet C, Dreifuss FE, Perret A, Wolf P (eds.). Epileptic syndromes in infancy, childhood and adolescense, 2 ed. John Libbey, 1992, 3-11.

Leppert M, Anderson VE, Quattlebaum T, Stauffer D, O’Connell P, Nakamura Y, Lalouel JM, White R. Benign familial neonatal convulsions linked to genetic markers on chromosome 20. Nature, 337:647-8, 1989.

Dravet C, Bureau M, Roger P. Benign myoclonic epilepsy in infants. In: Roger P, Bureau M, Dravet C, Dreifuss FE, Perret A, Wolf P (eds.). Epileptic syndromes in infancy, childhood and adolescense, 2 ed. John Libbey, 1992, 67-74.

Berg AT, Shinnar S, Hauser WA, Leventhal JM. Predictors of recurrent febrile seizures: A metaanalytic review. J Pediatr, 116:329-37, 1990.

Berg AT, Shinnar S, Hauser WA, Alemany M, Shapiro ED, Salomon ME, Grain EF. A prospective study of recurrent febrile seizures. N Engl J Med, 327:1122-7, 1992.

Knudsen FU. Recurrence risk after first febrile seizure and effect of short term diazepam prophylaxis. Arch Dis Child, 60:1045-9, 1985.

Maytal J, Shinnar S. Febrile Status Epilepticus. Pediatrics, 86:611-6, 1990.

Kramer U, Nevo Y, Neufeld MY, Fatal A, Leitner Y, Harel S. Epidemiology of epilepsy in childhood: a cohort of 440 consecutive patients. Pediatr Neurol, 18:46-50, 1998.

Miller SP, Dilenge ME, Meagher-Villemure K, O’Gorman AM, Shevell MI. Infantile epilepptic encephalopathy (Ohtahara syndrome) and migrational disorder. Pediatr Neurol, 19:50-4, 1998.

Williams AN, Gray RG, Poulton K, Ramani P, Whitehouse WP. A case of Ohtahara syndrome with cytocrome oxidase deficiency. Dev Med Child Neurol, 40:568-70, 1998.

Gonzalez De Dios J, Moya M, Pastore C, Izura V, Carratalà F. Early infantile epileptic encephalopathy and glycine encephalopathy. Rev Neurol, 25:1916-8, 1997.

Dravet C, Bureau M, Guerrini R, Giraldi N, Roger P. Severe myoclonic epilepsy in infants. In: Roger P, Bureau M, Dravet C, Dreifuss FE, Perret A, Wolf P (eds.). Epileptic syndromes in infancy, childhood and adolescense, 2 ed. John Libbey, 1992, 75-88.

Cowan LD, Hudson LS. The epidemiology and natural history of infantile spasms. J Child Neurol, 6:355-64, 1991.

Farrell K. Classifying epileptic syndromes: problems and a neurobiologic solution. Neurology, 43(suppl. 5):S8-S11, 1993.

Holmes GL. Surgery for intractable seizures in infancy and early childhood. Neurology, 43(suppl. 5):S28-S35, 1993.

Holmes GL. Intractable epilepsy in children. Epilepsia, 37(suppl. 3):14-25, 1996.

Kirkham FJ. Diagnosis, investigation and initiation of treatment in childhood epilepsies. In: Meldrum BS. Epilepsy. Ed. Pedley TA, Churchill Livingstone, 1995, cap. 8, pp. 139-71.

Shields WD. Investigational antiepileptic drugs for the treatment of childhood seizure disorders: a review of efficacy and safety. Epilepsia, 35(suppl. 2):S24-S29, 1994.

Pellock JM, Appleton R. Use of new antiepileptic drugs in the treatment of childhood epilepsy. Epilepsia, 40 (suppl. 6):S29-S38, 1999.

Holmes GL, Mckeever M, Adamson M. Absence seizures in children: clinical and electroencephalographic features. Annals of Neurology, 21:268-73, 1987.

Commission on classification and terminology of the international league against epilepsy. Proposal for revised clinical and electroencephalographic classification of epileptic seizures. Epilepsia, 22:489-501, 1981.

Olsson and Hedström. Epidemiology of absence epilepsy. Acta Pediatr Scand 80:235-42, 1991.

Porter RJ. The absence epilpsies. Epilepsia, 34(suppl. 3):S42- S8, 1993.

Degen R, Degen HE, Roth CH. Some genetic aspects of idiopathic and symptomatic absence seizures: Waking and sleep EEGs in siblings. Epilepsia, 31(6):784-94, 1990.

Oller-Daurella L, Oller FV. Epilepsy with generalized tonicclonic seizures in childhood. Does a childhood “grand mal” syndrome exist? In: Roger P, Bureau M, Dravet C, Dreifuss FE, Perret A, Wolf P (eds.). Epileptic syndromes in infancy, childhood and adolescense, 2 ed. John Libbey, 1992 pp. 161-71.

Beau Manoir A, Balls T, Varfis G, Ansari K. “Benign Epilepsy of childhood with Rolandic Spikes. Epilepsia, 15: 130-315, 1974.

Fejerman N, Caraballo R, Tenembaum SN. Atypical evolutions of benign localization-related epilepsies in children: are they predictable? Epilepsia, 41(4):380-90, 2000.

Gastaut H. A new type of epilepsy: benign partial epilepsy of childhood with occipital spike-waves. Clin Electroencephalogr, 13:13-22, 1982.

Talwar D, Rask CA, Torres F. Clinical manifestations in children with occipital spike-wave paroxysms. Epilepsia, 33(4):667-74, 1992.

Dalla Bernardina B, Chiament C, Capovilla G, Trevisan. E, Tassinari CA. Benign partial epilepsy with affective symptoms. In: Roger J, Dravet C, Bureau M, Dreifuss FE, Wolf P (eds.). Epileptic syndromes in infancy, childhood and adolescense. 2 ed. John Libbey, 1985, pp. 171-5.

Commission on classification and terminology of the international league against epilepsy proposal for revised classification of epilepsies and epileptic syndromes Epilepsia, 30(4):389-99, 1989.

Beaumanoir A & Dravet C. The Lennox-Gastaut syndrome. In: Roger J, Dravet C, Bureau M, Dreifuss FE, Perret A, Wolf P (eds.) Epileptic syndromes in infancy, childhood and adolescense. London: John Libbey, 1992, pp. 115 32.

Dulac O & N’ Guyen T. The Lennox-Gastaut syndrome. Epilepsia, 34(suppl. 7):S7-S17, 1993.

Shields WD. Catastrophic epilepsy in childhood. Epilepsia, 41(suppl. 2):S2-S6, 2000.

Doose H. Myoclonic astatic epilepsy of early childhood. In: Roger J, Dravet C, Bureau M, Dreifuss FE, Perret A, Wolf P. Epileptic Syndromes in Infancy, Childhood and Adolescense. London, John Libbey. 1992, pp. 103-14.

Muszkat M, Albuquerque M, Campos CJR. Juvenile Myoclonic Epilepsy (JME). Report of 12 cases. RHSP/EPM 2 (1/2), III 33-5, 1990.

Delgado-Escueta AV, Enrile-Bacsal F. Juvenile myoclonic epilepsy of Janz. Neurology, 34:285-94, 1984.

Devilat MB. “Epilepsia Mioclônica Juvenil” (Síndrome de Janz). Rev Child Pediatr, 60(5):275-9, 1989.

Grunewald RA, Chroni E, Panayiotopoulos CP. Delayed diagnosis of juvenile myoclonic epilepsy. J Neurol Neurosurg Psychiatry, 55:497-9, 1992.

Greenberg DA, Delgado-Escueta AV, Widlitz H. Juvenile myoclonic epilepsy may be linked to the BF and HLA loci on human chromosome 6. Am J Med Gen, 31:185-92, 1988.

Delgado-Escueta AV, Greenberg D, Weissbecker K. Gene mapping in the idiopathic generalized epilepsies: juvenile myoclonic epilepsy, childhood absence epilepsy, epilepsy with grand mal seizures, and early childhhood myoclonic epilepsy. Epilepsia, 31(suppl. 3):S19-S29, 1990.

Rogers SW, Andrews PI, Gahring LC, Whisenand T, Cauley K, Crain B, Hughes TE, Heinemann SF, McNamara JO. Autoantibodies to glutamate receptor GluR3 in Rasmussen’s Encephalitis. Science, 265(29):648-51, 1994.

Maria BL, Ringdahl DM, Mickle JP, Smith LJ, Reuman PD, Gilmore RL, Drane WE, Quisling RG. Intraventricular alpha interferon therapy for Rasmussen’s syndrome. Can J Neurol Sci, 20:333-6, 1993.

Privitera MD. Drug choices and sequences in generalizedonset epilepsies. In: American Academy of Neurology. Meeting April 25-May 1, New Yor, Vol. 1: Epilepsy, EEG, 245-63, 1993.

Published

2000-09-30

How to Cite

Rizzutti, S., Muszkat, M., & Vilanova, L. C. P. (2000). Childhood epilepsy. Revista Neurociências, 8(3), 108–116. https://doi.org/10.34024/rnc.2000.v8.8939

Issue

Section

Artigos Originais
##plugins.generic.dates.received## 2019-02-01
##plugins.generic.dates.published## 2000-09-30

Most read articles by the same author(s)

Obs.: This plugin requires at least one statistics/report plugin to be enabled. If your statistics plugins provide more than one metric then please also select a main metric on the admin's site settings page and/or on the journal manager's settings pages.

Similar Articles

1 2 3 4 5 6 7 8 9 10 > >> 

You may also start an advanced similarity search for this article.