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Neuropediatrics 2013; 44(03): 163-166
DOI: 10.1055/s-0032-1329613
Short Communication
Georg Thieme Verlag KG Stuttgart · New York

Paroxysmal Periodic Dystonic Postures in an Infant with 18q23 Deletion Syndrome

Nobustune Ishikawa
1   Department of Pediatrics, Hiroshima University Graduate School of Biomedical Sciences, Hiroshima, Japan
,
Yoshiyuki Kobayashi
1   Department of Pediatrics, Hiroshima University Graduate School of Biomedical Sciences, Hiroshima, Japan
,
Yuji Fujii
1   Department of Pediatrics, Hiroshima University Graduate School of Biomedical Sciences, Hiroshima, Japan
,
Masao Kobayashi
1   Department of Pediatrics, Hiroshima University Graduate School of Biomedical Sciences, Hiroshima, Japan
› Author Affiliations
Further Information

Publication History

31 March 2012

24 August 2012

Publication Date:
01 November 2012 (online)

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Abstract

The 18q23 deletion syndrome is characterized by diverse neurological and psychiatric features, including developmental delays, epilepsy, and autism. We report on a female infant with an 18q23 deletion who displayed atypical periodic dystonic postures. Video-electroencephalography recordings were used to evaluate the involuntary nonepileptic movements in the infant. Although nonepileptic involuntary movements have been rarely reported in adult patients, there are no reports of paroxysmal periodic dystonia in infants with 18q23 deletion. This study suggests that clustered periodic dystonia should be clinically recognized as a phenotypic feature in some patients with 18q23 deletion syndrome.

Keywords

18q23 deletion - involuntary movement - dystonic posture - video-EEG recording - tonic spasms
 

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