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Occipital lobe seizures: Rare hyperglycemic sequelae of type 1 diabetes mellitus

A 15-year-old boy presented with osmotic symptoms and photopsia. He had short-term memory impairment, visual hallucinations, and headache. His random blood sugar was 474 mg/dl, HbA1c −9.4%, and glutamic acid decarboxylase −65 >2000 IU/ml. Magnetic resonance imaging brain and cerebrospinal fluid s...

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Autores principales: Jalal, Muhammed Jasim Abdul, Menon, Murali Krishna, Kumar, K. Arun, Gomez, Ramesh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4770654/
https://www.ncbi.nlm.nih.gov/pubmed/26962348
http://dx.doi.org/10.4103/1817-1745.174449
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author Jalal, Muhammed Jasim Abdul
Menon, Murali Krishna
Kumar, K. Arun
Gomez, Ramesh
author_facet Jalal, Muhammed Jasim Abdul
Menon, Murali Krishna
Kumar, K. Arun
Gomez, Ramesh
author_sort Jalal, Muhammed Jasim Abdul
collection PubMed
description A 15-year-old boy presented with osmotic symptoms and photopsia. He had short-term memory impairment, visual hallucinations, and headache. His random blood sugar was 474 mg/dl, HbA1c −9.4%, and glutamic acid decarboxylase −65 >2000 IU/ml. Magnetic resonance imaging brain and cerebrospinal fluid study were normal. Digital electroencephalography was suggestive of bilateral hemispheric occipital lobe seizures. He responded well to insulin and antiepileptic medications.
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spelling pubmed-47706542016-03-09 Occipital lobe seizures: Rare hyperglycemic sequelae of type 1 diabetes mellitus Jalal, Muhammed Jasim Abdul Menon, Murali Krishna Kumar, K. Arun Gomez, Ramesh J Pediatr Neurosci Case Report A 15-year-old boy presented with osmotic symptoms and photopsia. He had short-term memory impairment, visual hallucinations, and headache. His random blood sugar was 474 mg/dl, HbA1c −9.4%, and glutamic acid decarboxylase −65 >2000 IU/ml. Magnetic resonance imaging brain and cerebrospinal fluid study were normal. Digital electroencephalography was suggestive of bilateral hemispheric occipital lobe seizures. He responded well to insulin and antiepileptic medications. Medknow Publications & Media Pvt Ltd 2015 /pmc/articles/PMC4770654/ /pubmed/26962348 http://dx.doi.org/10.4103/1817-1745.174449 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 ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Case Report
Jalal, Muhammed Jasim Abdul
Menon, Murali Krishna
Kumar, K. Arun
Gomez, Ramesh
Occipital lobe seizures: Rare hyperglycemic sequelae of type 1 diabetes mellitus
title Occipital lobe seizures: Rare hyperglycemic sequelae of type 1 diabetes mellitus
title_full Occipital lobe seizures: Rare hyperglycemic sequelae of type 1 diabetes mellitus
title_fullStr Occipital lobe seizures: Rare hyperglycemic sequelae of type 1 diabetes mellitus
title_full_unstemmed Occipital lobe seizures: Rare hyperglycemic sequelae of type 1 diabetes mellitus
title_short Occipital lobe seizures: Rare hyperglycemic sequelae of type 1 diabetes mellitus
title_sort occipital lobe seizures: rare hyperglycemic sequelae of type 1 diabetes mellitus
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4770654/
https://www.ncbi.nlm.nih.gov/pubmed/26962348
http://dx.doi.org/10.4103/1817-1745.174449
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