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Genomic Medicine and the Individual Patient—Byte to Bedside
A Call for Papers
Arch Intern Med. 2001;161:151.
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| Since this article does not have an abstract, we have provided the first 150 words of the full text and any section headings. |
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Why should any particular person be singled out to suffer a particular
disease? Patients ask, "Why me?" and the up-to-the-minute answer is provided
by the media, usually with pontifical certainty and authority, "It's in your
genes." And there is some truth in it.1
DESPITE THE current excitement and hubbub surrounding the mapping of
the human genome, the typical busy clinician heading for the examination room
is probably not thinking much about the role of genetics in the patient's
problem. The clinical relevance of the Human Genome Project2, 3
is evolving but far from being established. However, it seems likely that
the rapid accumulation of data on gene function will result in new approaches
to patient care both incrementally (eg, diagnostic testing) and globally by
"modifying medical thinking."1 Of course, genetic
testing is already central to the evaluation of some conditions, such as BRCA-related breast cancer.4
The term genomics (the systematic . . . [Full Text of this Article]
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ABSTRACT
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