J Korean Geriatr Soc.  2008 Mar;12(1):5-10.

Clinical Aspects of Genetic Testing for Dementia

Affiliations
  • 1Department of Neurology, College of Medicine, Kangwon National University, Kangwon, Korea.
  • 2Department of Neurology, College of Medicine, Korea University, Seoul, Korea. kunu@korea.ac.kr

Abstract

Dementia is the progressive or chronic dysfunction of cortical or subcortical functions that results in complex cognitive decline and Alzheimer's disease is the most common etiology of dementia. Currently, causal genetic mutations such as amyloid precursor protein, presenilin 1, presenilin 2 in familial Alzheimer's disease and many susceptible genes including polymorphysm of apolipoprotein E have been reported. Furthermore, genetic testings are available in person at risk for Alzheimer's disease. However, besides from results of genetic testing, there are many issues such as economics, ethics, psychological and legal. So clinician should be considered these complexities before ordering genetic test for patients with/without Alzheimer's disease.

Keyword

Familial Alzheimer's disease; Causal genes; Susceptible gene; Issues

MeSH Terms

Alzheimer Disease
Amyloid
Apolipoproteins
Dementia
Genetic Testing
Humans
Presenilin-1
Presenilin-2
Amyloid
Apolipoproteins
Presenilin-1
Presenilin-2
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