Probable early-onset Alzheimer's disease in an apolipoprotein E2 homozygote.

Abstract:

OBJECTIVE:To describe a case of early-onset Alzheimer's disease (AD) in an apolipoprotein (Apo) ε2/ε2 homozygote. BACKGROUND:Apo ε2/ε2 is the rarest of the ApoE genotypes, representing only 1.4% of the population. Cognitive decline in ApoE ε2 homozygotes has rarely been reported. CASE REPORT/METHODS:We report a 58-year-old Apo ε2/ε2 female who meets clinical criteria for probable AD as confirmed by neuropsychological testing, positron emission/computed tomography scan, CSF analysis and genetic screening for known mutations. RESULTS:The clinical course is typical of AD, with progressive cognitive and functional decline. CONCLUSION:Clinically confirmed early-onset AD is atypical in ApoE2 homozygotes but can occur.

authors

Cole L,Belden C,Jacobson S,Liebsack C,Myers K,Reninger C,Berk C,Sabbagh MN

doi

10.1159/000320589

subject

Has Abstract

pub_date

2010-01-01 00:00:00

pages

387-91

issue

5

eissn

1420-8008

issn

1421-9824

pii

000320589

journal_volume

30

pub_type

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