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Amniocentesis Test |
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Just what is the amniocentesis test and how it can help us diagnose
certain conditions during your pregnancy?

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Who should consider prenatal
testing and genetic counseling?
You are pregnant and will be 35 years of age or
older on your due date.
You are pregnant with an abnormal expanded AFP
blood test.
(Quad Test)
You have had an ultrasound of your fetus showing
a possible birth defect.
You have already had a child or close
relative with a birth defect or genetic disease.
You and your partner are carriers of a
recessively inherited disease such as Tay-Sachs, sickle cell anemia,
cystic fibrosis or thalassemia.
You are a carrier of an X linked disease such as
Fragile X, hemophilia or muscular dystrophy.
You and your partner are closely related to each
other (such as first cousins).
You have been exposed to medications, X-rays or
other agents during your pregnancy that may be harmful to the
developing fetus.
To fill out our online assessment form
click here
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We
are a group of Doctors and Professionals providing
sensitive and non-intrusive care. Innovation is the cornerstone of what we do and we
strive to be on the cutting edge of technology in order to
provide those answers.




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Both Drs. Thiagarajah and
Helmbrecht are widely published in their field and are considered
experts in the care and management of high risk pregnancies. Under
their expert guidance, The Prenatal Diagnosis Center offers the
earliest screening available for Down Syndrome and other
abnormalities in an unborn baby. They
perform first trimester screenings between 11 and 14 weeks of
gestation. The screening will detect up to 95 percent of Down syndrome
and other chromosome abnormalities. Drs. Thiagarajah and Helmbrecht
also perform second trimester ultrasounds, preferably at about 22
weeks’ gestation, to evaluate for fetal structural abnormalities.
Abnormalities of the fetal heart are among the most commonly
encountered in prenatal diagnosis. Those who are at increased risk
for a heart abnormality, such as diabetic mothers, those with a
previous child with a heart defect, those with a
family history of congenital heart disease or if they themselves
have a heart defect and exposure to certain
medications, can have a detailed evaluation of their baby’s heart
(echocardiogram) at 22 weeks gestation. Some fetal abnormalities
such as cleft lip are best illustrated using the new 3-D ultrasound
technology available at their office.
Couples referred to the Prenatal Diagnosis Center may receive
genetic counseling. Genetic counselors are trained in clinical genetics and counseling
and they have a Masters Degree in Genetic Counseling and extensive experience in providing information regarding
various genetic disorders. They are also trained in assisting with
the care of individuals carrying a pregnancy affected by a birth
defect as well as those at risk of a having a pregnancy with a birth
defect or genetic disorder.
Prior to their scheduled
ultrasound procedure, they meet with couples who are at increased
risk for fetal chromosomal and structural abnormalities to further
explain and clarify those risks. They take a detailed family and
medical history and discuss the ultrasound examination and other
possible tests. They will also discuss abnormal results and options
available to the families.
For more information about the
Center, talk with your healthcare provider or call us at:
434-220-8620 Fax: 434-220-8625
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Siva
Thiagarajah, M.D. Siva
Thiagarajah, M.D., is the medical director of the Prenatal Diagnosis
Center which is affiliated with Martha Jefferson Hospital.
His medical education includes
an Endocrinology and Infertility fellowship at the University of
Virginia, completed in 1970, and a residency in
Obstetrics/Gynecology, completed in 1974. In 1981, he
completed a fellowship in Maternal and Fetal Medicine at U.Va. He is
board certified in Obstetrics/Gynecology and also in Maternal-Fetal
Medicine. |
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Gary D
Helmbrecht, M.D.
Gary D. Helmbrecht, M.D. is board certified in
Obstetrics and Gynecology and Maternal-Fetal Medicine. His medical
education includes a Doctor of Medicine from the Medical College of
Wisconsin, Obstetrics and Gynecology residency at The National Naval
Medical Center in Bethesda, Maryland, and Fellowship in
Maternal-Fetal Medicine at Georgetown University Medical Center in
Washington, DC completed in 1994.
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Fotini
Vavelides, Genetic Counselor
Fotini Vavelidis has a master's degrees in human
genetics and genetic counseling from Sarah Lawrence College in New
York. She is certified by the American Board of Medical Genetics. She served as a genetics associate at the Children’s National
Medical Center in Washington, DC. She then was a member in the
Maternal-Fetal Medicine Division at UVA Medical Center before
joining our practice.
For more information about the
Center, talk with your healthcare provider or call us at:
434-220-8620 Fax: 434-220-8625. |
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