Document Detail


Progressive supranuclear palsy-like phenotype associated with bilateral hypoxic-ischemic striopallidal lesions.
MedLine Citation:
PMID:  15782420     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
A progressive supranuclear palsy (PSP)-like syndrome due to vascular or anoxic brain insult is rare. We describe a 65-year-old man with a progressive PSP-like phenotype associated with hypoxic-ischemic bilateral striopallidal lesions, secondary to rupture of and subsequent surgery for a thoracic aortic aneurysm. After early extrapyramidal features, 10 months later he started to fall, and developed levator inhibition. A supranuclear gaze palsy for downgaze was documented 5.5 years after the insult.
Authors:
Hee Tae Kim; Simon Shields; Kailash P Bhatia; Niall Quinn
Publication Detail:
Type:  Case Reports; Journal Article    
Journal Detail:
Title:  Movement disorders : official journal of the Movement Disorder Society     Volume:  20     ISSN:  0885-3185     ISO Abbreviation:  Mov. Disord.     Publication Date:  2005 Jun 
Date Detail:
Created Date:  2005-06-06     Completed Date:  2005-07-29     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  8610688     Medline TA:  Mov Disord     Country:  United States    
Other Details:
Languages:  eng     Pagination:  755-7     Citation Subset:  IM    
Copyright Information:
(c) 2005 Movement Disorder Society.
Affiliation:
National Hospital for Neurology and Neurosurgery, Queen Square, London, United Kingdom.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:
Aged
Corpus Striatum / pathology*
Humans
Hypoxia-Ischemia, Brain / complications*,  pathology*
Magnetic Resonance Imaging
Male
Supranuclear Palsy, Progressive / complications*,  pathology*

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


Previous Document:  New anticoagulants: a pediatric perspective.
Next Document:  Depressive symptoms and life satisfaction in patients with multiple system atrophy.