Alzheimer's disease presenting as corticobasal syndrome
Identifieur interne : 003597 ( Main/Exploration ); précédent : 003596; suivant : 003598Alzheimer's disease presenting as corticobasal syndrome
Auteurs : Pratap Chand [États-Unis] ; Jordan Grafman [États-Unis] ; Dennis Dickson [États-Unis] ; Keisuke Ishizawa [États-Unis] ; Irene Litvan [États-Unis]Source :
- Movement Disorders [ 0885-3185 ] ; 2006-11.
Descripteurs français
- Pascal (Inist)
English descriptors
- KwdEn :
- Alzheimer Disease (complications), Alzheimer Disease (metabolism), Alzheimer Disease (pathology), Alzheimer disease, Alzheimer's disease, Basal Ganglia Diseases (etiology), Basal Ganglia Diseases (pathology), Cerebral Amyloid Angiopathy (pathology), Degeneration, Functional Laterality, Hand (physiopathology), Humans, Male, Middle Aged, Myoclonus, Myoclonus (etiology), Nervous system diseases, Neurodegenerative Diseases (etiology), Neurodegenerative Diseases (metabolism), Neuropsychological Tests, Plaque, Amyloid (pathology), Supranuclear Palsy, Progressive (etiology), alien limb phenomenon, corticobasal degeneration, corticobasal syndrome, myoclonus, neuropathology, tau Proteins (metabolism).
- MESH :
- chemical , metabolism : tau Proteins.
- complications : Alzheimer Disease.
- etiology : Basal Ganglia Diseases, Myoclonus, Neurodegenerative Diseases, Supranuclear Palsy, Progressive.
- metabolism : Alzheimer Disease, Neurodegenerative Diseases.
- pathology : Alzheimer Disease, Basal Ganglia Diseases, Cerebral Amyloid Angiopathy, Plaque, Amyloid.
- physiopathology : Hand.
- Functional Laterality, Humans, Male, Middle Aged, Neuropsychological Tests.
Abstract
A 60‐year‐old man presented with slowly progressive left hemi‐Parkinsonism, left hand apraxia, myoclonus, dystonia, visuospatial disturbances, and alien limb phenomenon, resembling corticobasal syndrome. Eight years later, neuropathology revealed features of Alzheimer's disease, with asymmetrical (right more than left) cortical tau burden with image analysis. The videotaped clinical features, neuropsychological aspects, and neuropathological correlates are presented and discussed. © 2006 Movement Disorder Society
Url:
DOI: 10.1002/mds.21055
Affiliations:
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Le document en format XML
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<term>Alzheimer Disease (pathology)</term>
<term>Alzheimer disease</term>
<term>Alzheimer's disease</term>
<term>Basal Ganglia Diseases (etiology)</term>
<term>Basal Ganglia Diseases (pathology)</term>
<term>Cerebral Amyloid Angiopathy (pathology)</term>
<term>Degeneration</term>
<term>Functional Laterality</term>
<term>Hand (physiopathology)</term>
<term>Humans</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Myoclonus</term>
<term>Myoclonus (etiology)</term>
<term>Nervous system diseases</term>
<term>Neurodegenerative Diseases (etiology)</term>
<term>Neurodegenerative Diseases (metabolism)</term>
<term>Neuropsychological Tests</term>
<term>Plaque, Amyloid (pathology)</term>
<term>Supranuclear Palsy, Progressive (etiology)</term>
<term>alien limb phenomenon</term>
<term>corticobasal degeneration</term>
<term>corticobasal syndrome</term>
<term>myoclonus</term>
<term>neuropathology</term>
<term>tau Proteins (metabolism)</term>
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<keywords scheme="MESH" qualifier="etiology" xml:lang="en"><term>Basal Ganglia Diseases</term>
<term>Myoclonus</term>
<term>Neurodegenerative Diseases</term>
<term>Supranuclear Palsy, Progressive</term>
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<keywords scheme="MESH" qualifier="metabolism" xml:lang="en"><term>Alzheimer Disease</term>
<term>Neurodegenerative Diseases</term>
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<keywords scheme="MESH" qualifier="pathology" xml:lang="en"><term>Alzheimer Disease</term>
<term>Basal Ganglia Diseases</term>
<term>Cerebral Amyloid Angiopathy</term>
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<front><div type="abstract" xml:lang="en">A 60‐year‐old man presented with slowly progressive left hemi‐Parkinsonism, left hand apraxia, myoclonus, dystonia, visuospatial disturbances, and alien limb phenomenon, resembling corticobasal syndrome. Eight years later, neuropathology revealed features of Alzheimer's disease, with asymmetrical (right more than left) cortical tau burden with image analysis. The videotaped clinical features, neuropsychological aspects, and neuropathological correlates are presented and discussed. © 2006 Movement Disorder Society</div>
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<tree><country name="États-Unis"><region name="Kentucky"><name sortKey="Chand, Pratap" sort="Chand, Pratap" uniqKey="Chand P" first="Pratap" last="Chand">Pratap Chand</name>
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