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A Rare Case of Peripheral Nerve Hyperexcitability in Childhood: Isaacs Syndrome.

Authors :
Kanmaz S
Özcan M
Şimşek E
Serin HM
Aydogdu İ
Gökben S
Tekgül H
Source :
Journal of pediatric neurosciences [J Pediatr Neurosci] 2020 Apr-Jun; Vol. 15 (2), pp. 153-156. Date of Electronic Publication: 2020 Jun 27.
Publication Year :
2020

Abstract

Isaacs syndrome is rare disorder with peripheral nerve hyperexcitability syndromes with acquired neuromyotonia in childhood. We present a 13-year-old girl with muscle stiffness and neuromyotonia diagnosed Isaac syndrome with spontaneous discharge potentials on motor unit in electromyography and the diagnosis supported by the presence of antinuclear antibodies. A successful treatment was obtained using low-dose carbamazepine. Cause of Isaacs syndrome is unknown, generally thought to be an autoimmune etiology with voltage-gated potassium channelopathy; it sometimes occurs as a paraneoplastic syndrome. Early use of electromyography has critical role in the differential diagnosis with certain muscle disorders and peripheral nerve hyperexcitability syndromes.<br />Competing Interests: There are no conflicts of interest.<br /> (Copyright: © 2020 Journal of Pediatric Neurosciences.)

Details

Language :
English
ISSN :
1817-1745
Volume :
15
Issue :
2
Database :
MEDLINE
Journal :
Journal of pediatric neurosciences
Publication Type :
Academic Journal
Accession number :
33042252
Full Text :
https://doi.org/10.4103/jpn.JPN_128_19