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Journal of Medical Genetics 2000;37:135-138; doi:10.1136/jmg.37.2.135
Copyright © 2000 by the BMJ Publishing Group Ltd.
J Med Genet 2000;37:135-138 ( February )

Perspective

Shared decision making and non-directiveness in genetic counselling

Glyn Elwyna, Jonathon Grayb, Angus Clarkeb

a Department of Postgraduate Education for General Practice and Department of General Practice, University of Wales College of Medicine, Cardiff CF4 4XN, UK, b Institute of Medical Genetics, University of Wales College of Medicine, Cardiff CF4 4XN, UK

Correspondence to: Dr Elwyn, elwynG@cf.ac.uk

Revised version received 10 September 1999; Accepted for publication 18 September 1999

The first 150 words of the full text of this article appear below.

    Introduction

The term "genetic counselling" (GC) covers many different activities, but at its core it is a process of communication.1 It can refer to the diagnostic assessment of a child with multiple developmental problems. It can describe the facilitation of a decision making process in relation to predictive genetic testing for a late onset disorder. It can relate to a decision about prenatal diagnosis or the termination of a pregnancy at risk of a serious inherited disease. Topics discussed within GC can include plans for the continuing medical management of a person at risk of complications of a genetic disease, and can encompass whether or how to broach the topic of genetic disease with other members of the extended family.

The nature of the clinic discussion of these different elements of GC will vary greatly, and any one consultation is likely to entail a discussion of only one or a few . . . [Full text of this article]


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