A case of paroxysmal kinesigenic dyskinesia suspected to be reflex epilepsy.


Journal

Nagoya journal of medical science
ISSN: 2186-3326
Titre abrégé: Nagoya J Med Sci
Pays: Japan
ID NLM: 0412011

Informations de publication

Date de publication:
May 2021
Historique:
received: 24 08 2020
accepted: 29 09 2020
entrez: 9 7 2021
pubmed: 10 7 2021
medline: 15 12 2021
Statut: ppublish

Résumé

An 11-year-old male patient developed weakness or right arm elevation after sudden movement at the age of eight. Reflex epilepsy was initially suspected; however, magnetic resonance imaging and electroencephalography (EEG) revealed no abnormality. Video-EEG monitoring was performed, but no change was noted during attacks of weakness. He was diagnosed with paroxysmal kinesigenic dyskinesia (PKD) and carbamazepine has stopped his attacks. PKD is a rare neurological disorder characterized by brief attacks of involuntary movement triggered by sudden voluntary movements, which may be confused with reflex epilepsy. PKD should be considered as a differential diagnosis of reflex epilepsy.

Identifiants

pubmed: 34239184
doi: 10.18999/nagjms.83.2.361
pmc: PMC8236686
doi:

Types de publication

Case Reports

Langues

eng

Sous-ensembles de citation

IM

Pagination

361-365

Déclaration de conflit d'intérêts

There are no conflicts of interest.

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Auteurs

Chie Nakayama-Kamada (C)

Department of Neurosurgery, Sapporo Medical University, Sapporo, Japan.

Rei Enatsu (R)

Department of Neurosurgery, Sapporo Medical University, Sapporo, Japan.

Shinobu Fukumura (S)

Department of Pediatrics, Sapporo Medical University, Sapporo, Japan.

Tomoyoshi Kuribara (T)

Department of Neurosurgery, Sapporo Medical University, Sapporo, Japan.

Satoko Ochi (S)

Department of Neurosurgery, Sapporo Medical University, Sapporo, Japan.

Nobuhiro Mikuni (N)

Department of Neurosurgery, Sapporo Medical University, Sapporo, Japan.

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Classifications MeSH