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dc.contributor.authorTekturk, Pinar
dc.contributor.authorBAYKAL, Betül
dc.contributor.authorUYGUNER, Zehra Oya
dc.contributor.authorAydin-Ozemir, Zeynep
dc.date.accessioned2022-02-18T10:27:17Z
dc.date.available2022-02-18T10:27:17Z
dc.date.issued2014
dc.identifier.citationAydin-Ozemir Z., Tekturk P., UYGUNER Z. O. , BAYKAL B., "Galactosemia and phantom absence seizures", JOURNAL OF PEDIATRIC NEUROSCIENCES, cilt.9, sa.3, ss.253-256, 2014
dc.identifier.othervv_1032021
dc.identifier.otherav_9d46bf1b-821c-434e-8612-3ce9638a3b43
dc.identifier.urihttp://hdl.handle.net/20.500.12627/179269
dc.identifier.urihttps://doi.org/10.4103/1817-1745.147581
dc.description.abstractGeneralized and focal seizures can rarely be seen in galactosemia patients, but absence seizures were not reported previously. An 18-year-old male was diagnosed as galactosemia at the age of 8 months. No family history of epilepsy was present. His absence seizures realized at the age of 9 years. Generalized 3-4 Hz spike-wave discharges were identified in his electroencephalography. Homozygous mutation at exon 6 c. 563A > G was identified. The electroencephalogram of his sibling was unremarkable. Our aim was to present the long-term follow-up of a patient diagnosed with galactosemia, who had phantom absence seizures and typical 3-4 Hz spike-wave discharges in his electroencephalogram to draw attention to this rare association.
dc.language.isoeng
dc.subjectNeurology
dc.subjectNeurology (clinical)
dc.subjectLife Sciences
dc.subjectHealth Sciences
dc.subjectDahili Tıp Bilimleri
dc.subjectNöroloji
dc.subjectSağlık Bilimleri
dc.subjectTıp
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectKLİNİK NEUROLOJİ
dc.titleGalactosemia and phantom absence seizures
dc.typeMakale
dc.relation.journalJOURNAL OF PEDIATRIC NEUROSCIENCES
dc.contributor.departmentİstanbul Teknik Üniversitesi , ,
dc.identifier.volume9
dc.identifier.issue3
dc.identifier.startpage253
dc.identifier.endpage256
dc.contributor.firstauthorID3382345


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