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Benign Febrile Myoclonus in Childhood

Published online by Cambridge University Press:  02 December 2014

J.M. Dooley  and
J.D. Hayden
J.M. Dooley
Affiliation:
Division of Pediatric Neurology, Dalhousie University and IWK Health Centre, Halifax, Nova Scotia, Canada
J.D. Hayden
Affiliation:
Division of Pediatric Neurology, Dalhousie University and IWK Health Centre, Halifax, Nova Scotia, Canada
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Abstract

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Background:

Myoclonus is often associated with progressive myoclonic epilepsy or neurodegenerative conditions. Febrile myoclonus is a benign phenomenon, which has only been reported previously in one child.

Methods:

The clinical features of three children with fever-induced myoclonus are described.

Results:

Fever-induced myoclonus is characterized by frequent myoclonus, which resolves with resolution of the fever in otherwise healthy children.

Conclusion:

Recognition of fever-induced myoclonus as a benign phenomenon may prevent unnecessary investigations and interventions.

Conclusion:

Le fait de reconnaître le myoclonus induit par l'hyperthermie comme un phÉnomène bÉnin peut Éviter des investigations et des interventions inutiles.

Type
Other
Information
Canadian Journal of Neurological Sciences , Volume 31 , Issue 4 , November 2004 , pp. 504 - 505
Copyright
Copyright © The Canadian Journal of Neurological 2004

References

1. Rajakumar, K, Bodensteiner, JB. Febrile myoclonus: a survey of pediatric neurologists. Clin Pediatr 1996;35:331–332.CrossRefGoogle ScholarPubMed
2. Dooley, J, Gordon, K, Stewart, W. Autosomal dominant fever induced dystonia. Can J Neurol Sci 2001;28 (Suppl 2):S70.Google Scholar
3. Fenichel, GM. Clinical Pediatric Neurology: A Signs and Symptoms Approach. Philadelphia: WB Saunders, 2001:293–294.Google Scholar
4. Lam, SK, Chua, KB. Nipah virus encephalitis outbreak in Malaysia. Clin Infect Dis 2002;34 (Suppl 2):48–51.CrossRefGoogle ScholarPubMed
5. Bodensteiner, J. Stress-induced movement disorders. Clin Pediatr 2001;40:53–54.CrossRefGoogle ScholarPubMed
6. Aicardi, J. Myoclonic epilepsies of infancy and childhood. In: Fahn, S, Marsden, CD, Van Woert, M, (Eds). Advances in Neurology: Myoclonus. New York: Raven 1986;43:11–31.Google Scholar
7. Maegaki, Y, Akaboshi, S, Inagak, M, Takeshita, K. Unilateral involuntary movement associated with streptococcal infection: neurophysiological investigation. Neuropediatrics 2000;31:70–74.CrossRefGoogle ScholarPubMed
8. McMinn, P, Stratov, I, Nagarajan, L, Davis, S. Neurological manifestations of enterovirus 71 infection in children during an outbreak of hand, foot and mouth disease in Western Australia. Clin Infect Dis 2001;32:236–242.CrossRefGoogle ScholarPubMed
9. Bressman, S, Fahn, S. Essential myoclonus. In: Fahn, S, Marsden, CD, Van Woert, M, (Eds). Advances in Neurology: Myoclonus. New York: Raven 1986;43:287–294.Google ScholarPubMed
10. Janszky, J, Rasonyi, G, Halsz, P, et al. Disabling erratic myoclonus during lamotrigine therapy with high serum-level-report of 2 cases. Clin Neuropharmacol 2000;23:86–89.CrossRefGoogle Scholar
11. Asconape, J, Diedrich, A, Dellabadia, J. Myoclonus associated with the use of gabapentin. Epilepsia 2000; 4: 479–481.CrossRefGoogle Scholar
12. Lombroso, CT, Fejerman, N. Benign myoclonus of early infancy. Ann Neurol 1977;1:38–43.CrossRefGoogle ScholarPubMed
13. Morimoto, T, Yoshimatsu, M, Nagao, H, Matsuda, H. Three types of hyperthermic seizures in rats. Brain Dev 1992;14:53–57.CrossRefGoogle ScholarPubMed
14. Hommel, D, Heraud, JM, Hulin, A, Talarmin, A. Association of Tonate virus (subtype IIIB of the Venezuelan equine encephalitis complex) with encephalitis in a human. Clin Infect Dis 2000;30:188–190.CrossRefGoogle ScholarPubMed
15. Daube, JR, Peters, HL. Hereditary essential myoclonus. Arch Neurol 1966;15:587–594.CrossRefGoogle ScholarPubMed
16. Kempster, PA, Balla, JI. A clinical study of convulsive syncope. Clin Exp Neurol 1986;22:53–55.Google ScholarPubMed
17. Morrell, MJ. Differential diagnosis of seizures. Neurol Clin 1993;11:737–754.CrossRefGoogle ScholarPubMed
18. Oguni, H, Hayashi, K, Awaya, Y, Kukuyama, Y, Osawa, M. Severe myoclonic epilepsy in infants - a review based on the Tokyo Women’s Medical University series of 84 cases. Brain Dev 2001;23:736–748.CrossRefGoogle ScholarPubMed