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Galactosemia and phantom absence seizures

Generalized 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. Gen...

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Autores principales: Aydin-Özemir, Zeynep, Tektürk, Pınar, Uyguner, Zehra Oya, Baykan, Betül
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4302547/
https://www.ncbi.nlm.nih.gov/pubmed/25624930
http://dx.doi.org/10.4103/1817-1745.147581
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author Aydin-Özemir, Zeynep
Tektürk, Pınar
Uyguner, Zehra Oya
Baykan, Betül
author_facet Aydin-Özemir, Zeynep
Tektürk, Pınar
Uyguner, Zehra Oya
Baykan, Betül
author_sort Aydin-Özemir, Zeynep
collection PubMed
description Generalized 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.
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spelling pubmed-43025472015-01-26 Galactosemia and phantom absence seizures Aydin-Özemir, Zeynep Tektürk, Pınar Uyguner, Zehra Oya Baykan, Betül J Pediatr Neurosci Case Report Generalized 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. Medknow Publications & Media Pvt Ltd 2014 /pmc/articles/PMC4302547/ /pubmed/25624930 http://dx.doi.org/10.4103/1817-1745.147581 Text en Copyright: © Journal of Pediatric Neurosciences http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Aydin-Özemir, Zeynep
Tektürk, Pınar
Uyguner, Zehra Oya
Baykan, Betül
Galactosemia and phantom absence seizures
title Galactosemia and phantom absence seizures
title_full Galactosemia and phantom absence seizures
title_fullStr Galactosemia and phantom absence seizures
title_full_unstemmed Galactosemia and phantom absence seizures
title_short Galactosemia and phantom absence seizures
title_sort galactosemia and phantom absence seizures
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4302547/
https://www.ncbi.nlm.nih.gov/pubmed/25624930
http://dx.doi.org/10.4103/1817-1745.147581
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