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A
2-year old boy with a cardiac defect and developmental delay.
A 24-year
old man who needs to talk about his father's diagnosis of
hemochromatosis and what their genetic connection may mean
for his own health.
A 30-year
old woman of Ashkenazi Jewish descent who is not pregnant,
but is planning to have a child someday and wants to learn
more about Tay-Sachs disease, a genetic metabolic disorder.
A 45-year
old woman with Marfan syndrome who needs regular follow-up
and treatment for her genetic condition.
A 50-year
old man convalescing from his first heart attack, with coronary
artery disease in many relatives and concerns for his young
children.
These are just a few examples
of the kinds of people who visit the Clinical Genetics Program
of the Harvard-Partners Center for Genetics and Genomics.
The program offers
services to individuals with:
Known or suspected genetic conditions
A family history of a genetic
condition
An increased risk to be a carrier
of a genetic condition
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