test Browse by Author Names Browse by Titles of Works Browse by Subjects of Works Browse by Issue Dates of Works
       

Advanced Search
Home   
 
Browse   
Communities
& Collections
  
Issue Date   
Author   
Title   
Subject   
 
Sign on to:   
Receive email
updates
  
My Account
authorized users
  
Edit Profile   
 
Help   
About T-Space   

T-Space at The University of Toronto Libraries >
University of Toronto at Scarborough >
Bioline International Legacy Collection >
Bioline International Legacy Collection >

Please use this identifier to cite or link to this item: http://hdl.handle.net/1807/7752

Title: Case Report - Hallervorden Spatz disease: MR and pathological findings of a rare case
Authors: Sharma, M. C.
Aggarwal, N.
Bihari, M.
Goyal, V.
Gaikwed, S.
Vaishya, S.
Sarkar, C.
Keywords: Hallervorden Spatz disease, movement disorder, pantothenate kinase 2 deficiency
Issue Date: 31-Dec-2005
Publisher: Medknow Publications on behalf of the Neurological Society of India
Citation: Neurology India (ISSN: 0028-3886) Vol 53 Num 1
Abstract: We describe a child with pathologically proven Hallervorden Spatz disease. He presented with extrapyramidal symptoms and characteristic "eye-of-the-tiger" sign on magnetic resonance imaging. He was given the possible benefit if any of deep brain stimulation with no much improvement. Pathological examination of the brain showed iron deposition in bilateral globus pallidi, spongiform change and neuron axonal degeneration (spheroids).
URI: http://hdl.handle.net/1807/7752
Other Identifiers: http://www.bioline.org.br/abstract?id=ni05029
Rights: Copyright 2005 Neurology India.
Appears in Collections:Bioline International Legacy Collection

Files in This Item:

File Description SizeFormat
ni05029.pdf88.02 kBAdobe PDF
View/Open

Items in T-Space are protected by copyright, with all rights reserved, unless otherwise indicated.

uoft