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A Confusing Coincidence: Neonatal Hypoglycemic Seizures and Hyperekplexia
Hyperekplexia 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....
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3982260/ https://www.ncbi.nlm.nih.gov/pubmed/24782896 http://dx.doi.org/10.1155/2014/595412 |
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author | Demir, Nihat Doğan, Murat Yılmaz, Sanem Peker, Erdal Bulan, Keziban Tuncer, Oğuz |
author_facet | Demir, Nihat Doğan, Murat Yılmaz, Sanem Peker, Erdal Bulan, Keziban Tuncer, Oğuz |
author_sort | Demir, Nihat |
collection | PubMed |
description | Hyperekplexia 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. |
format | Online Article Text |
id | pubmed-3982260 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-39822602014-04-29 A Confusing Coincidence: Neonatal Hypoglycemic Seizures and Hyperekplexia Demir, Nihat Doğan, Murat Yılmaz, Sanem Peker, Erdal Bulan, Keziban Tuncer, Oğuz Case Rep Med Case Report Hyperekplexia 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. Hindawi Publishing Corporation 2014 2014-03-24 /pmc/articles/PMC3982260/ /pubmed/24782896 http://dx.doi.org/10.1155/2014/595412 Text en Copyright © 2014 Nihat Demir et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Demir, Nihat Doğan, Murat Yılmaz, Sanem Peker, Erdal Bulan, Keziban Tuncer, Oğuz A Confusing Coincidence: Neonatal Hypoglycemic Seizures and Hyperekplexia |
title | A Confusing Coincidence: Neonatal Hypoglycemic Seizures and Hyperekplexia |
title_full | A Confusing Coincidence: Neonatal Hypoglycemic Seizures and Hyperekplexia |
title_fullStr | A Confusing Coincidence: Neonatal Hypoglycemic Seizures and Hyperekplexia |
title_full_unstemmed | A Confusing Coincidence: Neonatal Hypoglycemic Seizures and Hyperekplexia |
title_short | A Confusing Coincidence: Neonatal Hypoglycemic Seizures and Hyperekplexia |
title_sort | confusing coincidence: neonatal hypoglycemic seizures and hyperekplexia |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3982260/ https://www.ncbi.nlm.nih.gov/pubmed/24782896 http://dx.doi.org/10.1155/2014/595412 |
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