Document Detail


Lennox-Gastaut syndrome and idiopathic intracranial hypertension.
MedLine Citation:
PMID:  20542434     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Lennox-Gastaut Syndrome is a severe childhood epilepsy syndrome characterised by the diagnostic triad of a slow spike and wave pattern on electroencephalogram, multiple seizure types and developmental delay. Idiopathic intracranial hypertension is a syndrome characterised by raised cerebrospinal fluid pressure in the absence of an intracranial mass lesion or ventricular dilatation and often headache. We present the first reported case of Lennox-Gastaut Syndrome associated with symptomatic idiopathic intracranial hypertension in a 15 year old male, requiring cerebrospinal fluid diversion by means of ventriculoperitoneal shunting.
Authors:
Jason A Correia; Patrick M Schweder; Peter J Mews; Rakesh Patel; Andrew J J Law
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Publication Detail:
Type:  Case Reports; Journal Article     Date:  2010-06-12
Journal Detail:
Title:  Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia     Volume:  17     ISSN:  1532-2653     ISO Abbreviation:  J Clin Neurosci     Publication Date:  2010 Sep 
Date Detail:
Created Date:  2010-07-30     Completed Date:  2011-01-28     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  9433352     Medline TA:  J Clin Neurosci     Country:  Scotland    
Other Details:
Languages:  eng     Pagination:  1208-9     Citation Subset:  IM    
Copyright Information:
Copyright 2010. Published by Elsevier Ltd.
Affiliation:
Department of Paediatric Neurosurgery, Starship Children's Hospital, Park Road, Grafton, Auckland, New Zealand. jason_correia@yahoo.com
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MeSH Terms
Descriptor/Qualifier:
Adolescent
Epilepsy / complications*,  diagnosis*,  surgery
Humans
Male
Pseudotumor Cerebri / complications*,  diagnosis*,  surgery
Syndrome
Ventriculoperitoneal Shunt

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