CHROMOSOME 14-ENCODED ALZHEIMERS-DISEASE - GENETIC AND CLINICOPATHOLOGICAL DESCRIPTION

被引:89
作者
HALTIA, M
VIITANEN, M
SULKAVA, R
ALAHURULA, V
POYHONEN, M
GOLDFARB, L
BROWN, P
LEVY, E
HOULDEN, H
CROOK, R
GOATE, A
CLARK, R
KORENBLAT, K
PANDIT, S
KELLER, HD
LILIUS, L
LIU, L
AXELMAN, K
FORSELL, L
WINBLAD, B
LANNFELT, L
HARDY, J
机构
[1] UNIV S FLORIDA,DEPT PSYCHIAT,SUNCOAST ALZHEIMERS DIS LABS,TAMPA,FL 33613
[2] UNIV HELSINKI,DEPT PATHOL,HELSINKI,FINLAND
[3] KAROLINSKA INST,DEPT CLIN NEUROSCI,HUDDINGE,SWEDEN
[4] UNIV KUOPIO,DEPT COMMUNITY HLTH & GEN PRACTICE,SF-70211 KUOPIO,FINLAND
[5] KEMI CENT HOSP,DEPT NEUROL,KEMI,FINLAND
[6] OULU UNIV HOSP,DEPT CLIN GENET,OULU,FINLAND
[7] NIH,CENT NERVOUS SYST STUDIES LAB,BETHESDA,MD 20892
[8] NYU,MED CTR,DEPT PATHOL,NEW YORK,NY 10016
[9] NYU,MED CTR,DEPT PHARMACOL,NEW YORK,NY 10016
[10] UNIV S FLORIDA,DEPT PHARMACOL,TAMPA,FL
[11] UNIV S FLORIDA,DEPT NEUROL,TAMPA,FL 33620
[12] WASHINGTON UNIV,SCH MED,DEPT PSYCHIAT,ST LOUIS,MO 63110
[13] WASHINGTON UNIV,SCH MED,DEPT SURG,DIV HUMAN GENET,ST LOUIS,MO 63110
[14] ST MARYS HOSP,SCH MED,DEPT BIOCHEM,PRION GRP,LONDON,ENGLAND
[15] ST MARYS HOSP,SCH MED,DEPT BIOCHEM,DEMENTIA RES GRP,LONDON,ENGLAND
[16] ST MARYS HOSP,SCH MED,DEPT NEUROL,LONDON,ENGLAND
关键词
D O I
10.1002/ana.410360307
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
A family of Finnish descent with very-early-onset Alzheimer's disease has been identified. Genetic analysis of this family eliminated the amyloid precursor protein gene as the pathogenic locus, but strongly implicated a locus on chromosome 14q23.4 between D14S52 and D14S55. The early age at onset of the disease (average, 36 years; range, 35-39 years), the rapid progression, and the early and prominent myoclonus, while they appear to be frequent findings in the chromosome 14-encoded form of Alzheimer's disease, raised the clinical suspicion of prion disease. However, sequencing the prion gene-coding region of 2 affected members of the pedigree failed to show any abnormality. Apart from the presence of modest cortical vacuolar change, the pathological features of our index patient appeared typical of Alzheimer's disease with abundant senile plaques immunoreactive with beta-amyloid, but not with prion protein antibodies.
引用
收藏
页码:362 / 367
页数:6
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