The diagnosis of young-onset dementia

被引:393
作者
Rossor, Martin N. [1 ]
Fox, Nick C. [1 ]
Mummery, Catherine J. [1 ]
Schott, Jonathan M. [1 ]
Warren, Jason D. [1 ]
机构
[1] UCL, Inst Neurol, Dept Neurodegenerat, Dementia Res Ctr, London WC1N 3BG, England
基金
英国医学研究理事会; 美国国家卫生研究院;
关键词
FAMILIAL ALZHEIMERS-DISEASE; COGNITIVE IMPAIRMENT; SPASTIC PARAPARESIS; BRAIN ATROPHY; VARIANT; ENCEPHALOPATHY; PREVALENCE; MANAGEMENT; MUTATIONS; CRITERIA;
D O I
10.1016/S1474-4422(10)70159-9
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
A diagnosis of dementia is devastating at any age but diagnosis in younger patients presents a particular challenge. The differential diagnosis is broad as late presentation of metabolic disease is common and the burden of inherited dementia is higher in these patients than in patients with late-onset dementia. The presentation of the common degenerative diseases of late life, such as Alzheimer's disease, can be different when presenting in the fifth or sixth decade. Moreover, many of the young-onset dementias are treatable. The identification of causative genes for many of the inherited degenerative dementias has led to an understanding of the molecular pathology, which is also applicable to later-onset sporadic disease. This understanding offers the potential for future treatments to be tailored to a specific diagnosis of both young-onset and late-onset dementia.
引用
收藏
页码:793 / 806
页数:14
相关论文
共 81 条
[1]   SUBCORTICAL DEMENTIA OF PROGRESSIVE SUPRANUCLEAR PALSY [J].
ALBERT, ML ;
FELDMAN, RG ;
WILLIS, AL .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 1974, 37 (02) :121-130
[2]   Ataxic variant of Alzheimer's disease caused by Pro117Ala PSEN1 mutation [J].
Anheim, M. ;
Hannequin, D. ;
Boulay, C. ;
Martin, C. ;
Campion, D. ;
Tranchant, C. .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 2007, 78 (12) :1414-1415
[3]  
[Anonymous], PRACT NEUROL
[4]  
[Anonymous], 2000, DIAGN STAT MAN MENT, DOI DOI 10.1176/APPI.BOOKS.9780890425787
[5]   Pure spastic paraparesis associated with a novel presenilin 1 R278K mutation [J].
Assini, A ;
Terreni, L ;
Borghi, R ;
Giliberto, L ;
Piccini, A ;
Loqui, D ;
Fogliarino, S ;
Forloni, G ;
Tabaton, M .
NEUROLOGY, 2003, 60 (01) :150-151
[6]   POSTERIOR CORTICAL ATROPHY [J].
BENSON, DF ;
DAVIS, RJ ;
SNYDER, BD .
ARCHIVES OF NEUROLOGY, 1988, 45 (07) :789-793
[7]   ASSOCIATION BETWEEN QUANTITATIVE MEASURES OF DEMENTIA AND OF SENILE CHANGE IN CEREBRAL GREY MATTER OF ELDERLY SUBJECTS [J].
BLESSED, G ;
TOMLINSON, BE ;
ROTH, M .
BRITISH JOURNAL OF PSYCHIATRY, 1968, 114 (512) :797-+
[8]   Is early-onset clinically different from late-onset frontotemporal dementia? [J].
Borroni, B. ;
Agosti, C. ;
Bellelli, G. ;
Padovani, A. .
EUROPEAN JOURNAL OF NEUROLOGY, 2008, 15 (12) :1412-1415
[9]   Mutation within TARDBP Leads to Frontotemporal Dementia without Motor Neuron Disease [J].
Borroni, B. ;
Bonvicini, C. ;
Alberici, A. ;
Buratti, E. ;
Agosti, C. ;
Archetti, S. ;
Papetti, A. ;
Stuani, C. ;
Di Luca, M. ;
Gennarelli, M. ;
Padovani, A. .
HUMAN MUTATION, 2009, 30 (11) :E974-E983
[10]   Cognitive deficits associated with a recently reported familial neurodegenerative disease - Familial encephalopathy with neuroserpin inclusion bodies [J].
Bradshaw, CB ;
Davis, RL ;
Shrimpton, AE ;
Holohan, PD ;
Rea, CB ;
Fieglin, D ;
Kent, P ;
Collins, GH .
ARCHIVES OF NEUROLOGY, 2001, 58 (09) :1429-1434