The clinical and neuropathological features of sporadic (Late-onset) and genetic forms of alzheimer's disease

The purpose of this review is to compare and highlight the clinical and pathological aspects of genetic versus acquired Alzheimer's disease: Down syndrome-associated Alzheimer's disease in (DSAD) and Autosomal Dominant Alzheimer's disease (ADAD) are compared with the late-onset form o...

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Detalles Bibliográficos
Autores: Rujeedawa, Tanzil|||0000-0002-7089-1684, Carrillo Félez, Eva, Clare, Isabel C.H.|||0000-0002-5385-008X, Fortea, Juan|||0000-0002-1340-638X, Strydom, Andre, Rebillat, Anne-Sophie|||0000-0003-1995-9177, Coppus, Antonia, Levin, Johannes|||0000-0001-5092-4306, Zaman, Shahid
Tipo de recurso: artículo
Fecha de publicación:2021
País:España
Institución:Universitat Autònoma de Barcelona
Repositorio:Dipòsit Digital de Documents de la UAB
Idioma:inglés
OAI Identifier:oai:ddd.uab.cat:272142
Acceso en línea:https://ddd.uab.cat/record/272142
https://dx.doi.org/urn:doi:10.3390/jcm10194582
Access Level:acceso abierto
Palabra clave:Late-onset Alzheimer's disease
Down syndrome
Autosomal dominant Alzheimer's disease
Clinical features
Neuropathology
Descripción
Sumario:The purpose of this review is to compare and highlight the clinical and pathological aspects of genetic versus acquired Alzheimer's disease: Down syndrome-associated Alzheimer's disease in (DSAD) and Autosomal Dominant Alzheimer's disease (ADAD) are compared with the late-onset form of the disease (LOAD). DSAD and ADAD present in a younger population and are more likely to manifest with non-amnestic (such as dysexecutive function features) in the prodromal phase or neurological features (such as seizures and paralysis) especially in ADAD. The very large variety of mutations associated with ADAD explains the wider range of phenotypes. In the LOAD, age-associated comorbidities explain many of the phenotypic differences.