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Review Article

Free Access

The Role of Genetics in Delirium in the Elderly Patient

van Munster B.C.a, b · de Rooij S.E.b · Korevaar J.C.a

Author affiliations

aDepartment of Clinical Epidemiology, Biostatistics and Bioinformatics, and bDepartment of Internal Medicine, Academic Medical Centre, Amsterdam, The Netherlands

Corresponding Author

B.C. van Munster

Department of Clinical Epidemiology, Biostatistics and Bioinformatics

Room J1B-207-1, Academic Medical Centre, University of Amsterdam, PO Box 22660

NL–1100 DD Amsterdam (The Netherlands)

Tel. +31 20 566 6945, Fax +31 20 691 2683, E-Mail b.c.vanmunster@amc.uva.nl

Related Articles for ""

Dement Geriatr Cogn Disord 2009;28:187–195

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Delirium is an important neuropsychiatric syndrome in the elderly that is associated with an increase in mortality, impaired physical and cognitive recovery, and increased healthcare costs. Two important gaps in daily practice with delirium are the pathophysiological obscurity and the low recognition rates. Genetics offers the possibility to contribute knowledge to both of these gaps with its unique and diverse techniques. However, genetic studies in delirium have been scarce until recently, due to the nature of the diagnosis, the etiology of the syndrome, and the pitfalls inherent in the design of genetic studies. This review describes the barriers of this field of research and the implications for our current knowledge of delirium.

© 2009 S. Karger AG, Basel

Article / Publication Details

First-Page Preview
Abstract of Review Article

Accepted: May 29, 2009
Published online: August 28, 2009
Issue release date: October 2009

Number of Print Pages: 9
Number of Figures: 1
Number of Tables: 2

ISSN: 1420-8008 (Print)
eISSN: 1421-9824 (Online)

For additional information: http://www.karger.com/DEM

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