| What is Presymptomatic Testing?
Presymptomatic testing is a method for identifying persons carrying
the HD gene before symptoms appear. In the past, no laboratory test
could positively identify people carrying the HD gene--or those
fated to develop HD--before the onset of symptoms. That situation
changed in 1983, when a team of scientists supported by the NINDS
located the first genetic marker for HD--the initial step in developing
a laboratory test for the disease.
A marker is a piece of DNA that lies near a gene and is usually
inherited with it. Discovery of the first HD marker allowed scientists
to locate the HD gene on chromosome 4. The marker discovery quickly
led to the development of a presymptomatic test for some individuals,
but this test required blood or tissue samples from both affected
and unaffected family members in order to identify markers unique
to that particular family. For this reason, adopted individuals,
orphans, and people who had few living family members were unable
to use the test.
Discovery of the HD gene has led to a less expensive, scientifically
simpler, and far more accurate presymptomatic test that is applicable
to the majority of at-risk people. The new test uses CAG repeat
length to detect the presence of the HD mutation in blood. This
is discussed further in the next section.
In a small number of individuals with HD--1 to 3 percent--no family
history of HD can be found. Some individuals may not be aware of
their genetic legacy, or a family member may conceal a genetic disorder
from fear of social stigma. A parent may not want to worry children,
scare them, or deter them from marrying. In other cases, a family
member may die of another cause before he or she begins to show
signs of HD. Sometimes, the cause of death for a relative may not
be known, or the family is not aware of a relative's death. Adopted
children may not know their genetic heritage, or early symptoms
in an individual may be too slight to attract attention. These are
among the many complicating factors that reflect the complexity
of diagnosing HD.
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