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Welcome to the home page for the Prenatal Genetics and Fetal Therapy
Program at the University of Washington.
We are a multidisciplinary, reproductive genetics center that provides comprehensive fetal assessment and treatment for pregnant patients and those planning a pregnancy. Our services are provided by:
- Maternal Fetal Medicine Specialists
- Genetic Counselors/Geneticists
- Neonatologists
- Radiologists
- Pediatric Surgeons
- Pediatric Cardiologists
We offer full laboratory support, including cytogenetics, DNA, immunology and pathology services.
Our Mission:
To provide all patients or families who request or need it, a comprehensive,
high quality genetic counseling and prenatal diagnosis service.
Who may be interested in genetic counseling?
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Couples who have been identified as carrying a gene for a genetic disease
- All pregnant women interested in having a first or second trimester genetic risk assessment, including serum screening and ultrasound.
- Couples or individuals with a family history of inherited diseases such
as spina bifida or cystic fibrosis
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Couples or individuals with a history of repeated pregnancy loss or stillbirths
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Couples or individuals who have previously given birth to a child with
a genetic disease or birth defect
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Women 35 or older, and men 55 or older
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Women with abnormal ultrasounds, positive serum screens or current or
prior fetuses affected by chromosomal abnormalities
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Women who have specific concerns about exposures to certain drugs, chemicals
or infection during pregnancy
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Anyone with questions or concerns about risks in their pregnancy
What services are available?
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Genetic risk assessment and counseling
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First trimester prenatal screening
- Nuchal translucency ultrasound assessment
- 1st trimester serum screening
- Second trimester serum screening
- Integrated consultation and case management by maternal fetal medicine and pediatric specialists
- Targeted and serial ultrasound for fetal anatomy
- Prenatal diagnosis procedures
- Chorionic villus sampling
- Amniocentesis
- Fetal therapies:
- Congenital adrenal hyperplasia
- Bladder outlet obstruction
- Rh isoimmunication
- Twin/twin transfusion
What does genetic counseling involve?
The Prenatal Diagnosis Program consists of a group of specially trained
genetic counselors, obstetricians, ultrasonographers and laboratory personnel.
This service is designed to help people understand their risks of having
a child with a birth defect and to learn more about their options so that
they may make more informed decisions about their baby. |