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Genetics
Genetics at
the Center for Children is dedicated to diagnosing and counseling
patients with conditions that may be the result of genetics. A
team -- consisting of a clinical geneticist, genetic counselor
and an administrative staff member -- provides diagnostic services,
treatment and prevention programs to reduce the risk and severity
of disabling conditions.
Patients who might be referred for genetic evaluation or counseling
include those with the following:
A family history of mental retardation, birth defects,
neural tube defects or suspected genetic conditions.
A child with a known or suspected genetic condition,
mental retardation, developmental delays, autism or birth defects.
A child with physical abnormalities, growth problems,
developmental problems, or puberty problems.
Two or more unexplained pregnancy losses including miscarriage
and/or stillbirth or with infertility problems.
Members of certain ethnic groups, which place them at
increased risk of having a child with a genetic condition.
Marriages with or plan to marry blood relatives (consanguinity).
Prenatal screening tests (Maternal Serum Screen or ultrasound)
that have indicated an increased risk for birth defects.
Pregnant at or after 35 years old.
Questions about genetics and prenatal diagnosis.
Genetics is
committed to diagnosing heritable conditions; counseling individuals
and families and supporting their health care providers; researching
the causes of genetic diseases in order to prevent future disabling
conditions; and educating healthcare providers, teachers and the
public about genetics.
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