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dc.contributor.authorSwearer, Joan M.
dc.contributor.authorO'Donnell, Brian F.
dc.contributor.authorDrachman, David A.
dc.contributor.authorWoodward, Beatrice M.
dc.date2022-08-11T08:09:27.000
dc.date.accessioned2022-08-23T16:31:28Z
dc.date.available2022-08-23T16:31:28Z
dc.date.issued1992-11-01
dc.date.submitted2009-06-02
dc.identifier.citation<p>Ann Neurol. 1992 Nov;32(5):687-94. <a href="http://dx.doi.org/10.1002/ana.410320513">Link to article on publisher's site</a></p>
dc.identifier.issn0364-5134 (Print)
dc.identifier.doi10.1002/ana.410320513
dc.identifier.pmid1449250
dc.identifier.urihttp://hdl.handle.net/20.500.14038/37653
dc.description.abstractIt has been proposed that early-onset familial Alzheimer's disease (FAD) and sporadic Alzheimer's disease (AD) have different causes, with FAD due to a single dominant gene with disease onset before the sixth decade, whereas sporadic AD has a later onset and is not associated with a dominant pattern of inheritance. Given these differences, we questioned whether these etiologically distinct forms of AD also differ neuropsychologically. In this study we performed neuropsychological evaluations on patients from two well-documented families with FAD and a group of patients with sporadic AD. The groups were matched on global disease severity at entry. Two groups of education- and age-matched normal controls were recruited for comparison. The groups were analyzed for psychometric findings and pattern of deficits. Both patients with FAD and patients with sporadic AD showed a similar pattern of neuropsychological impairment relative to age-matched controls, i.e., mildly to moderately impaired verbal performance and concentration, severely slowed psychomotor speed, and severely impaired delayed recall of verbal material. There were no differences in pattern suggestive of disproportionately severe anomia, amnesia, agnosia, or apraxia in the early onset FAD group, as has been reported previously.
dc.language.isoen_US
dc.relation<p><a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=1449250&dopt=Abstract">Link to Article in PubMed</a></p>
dc.relation.urlhttps://doi.org/10.1002/ana.410320513
dc.subjectAdult
dc.subjectAged
dc.subjectAged, 80 and over
dc.subjectAlzheimer Disease
dc.subjectCognition Disorders
dc.subjectFamily
dc.subjectFemale
dc.subjectHumans
dc.subjectLanguage Disorders
dc.subjectMale
dc.subjectMemory
dc.subjectMiddle Aged
dc.subject*Neuropsychological Tests
dc.subjectPedigree
dc.subjectNeurology
dc.subjectNeuroscience and Neurobiology
dc.titleNeuropsychological features of familial Alzheimer's disease
dc.typeJournal Article
dc.source.journaltitleAnnals of neurology
dc.source.volume32
dc.source.issue5
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/neuro_pp/203
dc.identifier.contextkey861162
html.description.abstract<p>It has been proposed that early-onset familial Alzheimer's disease (FAD) and sporadic Alzheimer's disease (AD) have different causes, with FAD due to a single dominant gene with disease onset before the sixth decade, whereas sporadic AD has a later onset and is not associated with a dominant pattern of inheritance. Given these differences, we questioned whether these etiologically distinct forms of AD also differ neuropsychologically. In this study we performed neuropsychological evaluations on patients from two well-documented families with FAD and a group of patients with sporadic AD. The groups were matched on global disease severity at entry. Two groups of education- and age-matched normal controls were recruited for comparison. The groups were analyzed for psychometric findings and pattern of deficits. Both patients with FAD and patients with sporadic AD showed a similar pattern of neuropsychological impairment relative to age-matched controls, i.e., mildly to moderately impaired verbal performance and concentration, severely slowed psychomotor speed, and severely impaired delayed recall of verbal material. There were no differences in pattern suggestive of disproportionately severe anomia, amnesia, agnosia, or apraxia in the early onset FAD group, as has been reported previously.</p>
dc.identifier.submissionpathneuro_pp/203
dc.contributor.departmentDepartment of Psychiatry
dc.contributor.departmentDepartment of Neurology
dc.source.pages687-94


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