Publication:
Propriospinal Myoclonus in a Child

dc.authorscopusid55412732700
dc.authorscopusid8281689900
dc.authorscopusid25929913700
dc.authorscopusid9841285300
dc.authorscopusid6603156640
dc.contributor.authorAydin, T.F.
dc.contributor.authorTemuçin, C.M.
dc.contributor.authorKayacik, Ö.E.
dc.contributor.authorTürker, H.
dc.contributor.authorÖzyürek, H.
dc.date.accessioned2020-06-21T14:47:47Z
dc.date.available2020-06-21T14:47:47Z
dc.date.issued2010
dc.departmentOndokuz Mayıs Üniversitesien_US
dc.department-temp[Aydin] Ömer Faruk, Department of Pediatric Neurology, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Temuçin] Çağrı Mesut, Department of Neurology, Hacettepe Üniversitesi, Ankara, Turkey; [Kayacik] Özlem Eroǧlu, Department of Pediatric Neurology, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Türker] Hande Y., Department of Neurology, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Özyürek] Hamit, Department of Pediatric Neurology, Ondokuz Mayis Üniversitesi, Samsun, Turkeyen_US
dc.description.abstractA 6-year-old girl was experiencing repetitive involuntary and massive jerks immediately involving limbs and trunk. The first motor events appeared approximately at 1 year old and only 5 months after a back trauma. Myoclonus became progressively more frequent and more violent, causing episodes of falls. Neurological examination showed jerks characterized by upper limb abduction, lower limb abduction, and head-body hyperextension. Apart from these motor events, the neurological examination was normal. The results of vitamin B <inf>12</inf> and folate, antinuclear antibody, anti-DNA, anti-Tiroglobulin, anti-thyroid peroxidase antibody, lupus anticoagulant, anti-cardiolipin antibody, rheumatoid factor, and C3 and C4 were unexceptional. Electroencephalography and brain and spinal magnetic resonance imaging were unremarkable. Electromyographic records with surface electrodes showed that duration of myoclonic jerks was ranging from 100 to 300 ms. We thought she had propriospinal myoclonus because of presence of the spreading through the shoulder, upper limbs, and lower limbs in addition to thoracolumbar paraspinal muscles. © The Author(s) 2010.en_US
dc.identifier.doi10.1177/0883073809343610
dc.identifier.endpage915en_US
dc.identifier.issn0883-0738
dc.identifier.issn1708-8283
dc.identifier.issue7en_US
dc.identifier.pmid20197268
dc.identifier.scopus2-s2.0-77954402616
dc.identifier.scopusqualityQ2
dc.identifier.startpage912en_US
dc.identifier.urihttps://doi.org/10.1177/0883073809343610
dc.identifier.volume25en_US
dc.identifier.wosWOS:000279409100019
dc.identifier.wosqualityQ2
dc.language.isoenen_US
dc.publisherSAGE Publications Inc.en_US
dc.relation.ispartofJournal of Child Neurologyen_US
dc.relation.journalJournal of Child Neurologyen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectElectromyographyen_US
dc.subjectPropriospinal Myoclonusen_US
dc.subjectSpinal Myoclonusen_US
dc.subjectStimulo-Sensitiveen_US
dc.titlePropriospinal Myoclonus in a Childen_US
dc.typeArticleen_US
dspace.entity.typePublication

Files