A confusing coincidence: Neonatal hypoglycemic seizures and hyperekplexia

Basit Öğe Kaydı
dc.contributor.authorDemir N.
dc.contributor.authorDogan M.
dc.contributor.authorYlmaz S.
dc.contributor.authorPeker E.
dc.contributor.authorBulan K.
dc.contributor.authorTuncer O.
dc.date.accessioned2019-10-26T21:30:38Z
dc.date.available2019-10-26T21:30:38Z
dc.date.issued2014
dc.departmentEge Üniversitesien_US
dc.description.abstractHyperekplexia is a rare, nonepileptic, genetic, or sporadic neurologic disorder characterized by startle responses to acoustic, optic, or tactile stimuli. Genetic defects in glycine receptors as well as encephalitis, tumors, inflammation, and disgenesis are among the etiologic causes of the disease. The main problem in hyperekplexia is the incomplete development of inhibitory mechanisms or exaggerated stimulation of excitatory mediators. Hyperekplexia is often confused with epileptic seizures. Here we present a case with hypoglycemic convulsions coexisting with hyperekplexia, causing diagnostic difficulty. © 2014 Nihat Demir et al.en_US
dc.identifier.doi10.1155/2014/595412
dc.identifier.issn1687-9627
dc.identifier.issn1687-9627en_US
dc.identifier.scopusqualityQ4en_US
dc.identifier.urihttps://doi.org/10.1155/2014/595412
dc.identifier.urihttps://hdl.handle.net/11454/17640
dc.identifier.volume2014en_US
dc.indekslendigikaynakScopusen_US
dc.language.isoenen_US
dc.publisherHindawi Limiteden_US
dc.relation.ispartofCase Reports in Medicineen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.titleA confusing coincidence: Neonatal hypoglycemic seizures and hyperekplexiaen_US
dc.typeArticleen_US

Dosyalar

Koleksiyon

Scopus İndeksli Yayınlar Koleksiyonu