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Double Marker Screening with Preeclampsia.
Double Marker Screening with Preeclampsia.
First trimester maternal serum based double marker test is done at 11-13 wks of gestation. Down Syndrome and other common aneuploidy risk is calculated by testing two biochemical markers PAPP-A, beta-hCG and PLGF along with ultrasound markers such as NT/CRL and nasal bone.
3500
₹2599
76% OFF
2 weeks
Schedule test now
Schedule test now
Sample Collection and Transportation
Sample Collection: 3ml Peripheral Blood in PURPLE TOP (EDTA) Vacutainer Transport within 48 hrs at room temperature
Download Brochure
Alternate Names
First trimester screening with preeclampsia, FTS with preeclampsis, Double marker testwith preeclampsia, FTS + PLGF, Double marker with Placental Growth Factor
Specialities
ObGyn, IVF, Fetal Medicine
Technology
The biochemical markers PAPP-A, beta-hCG and PLGF are analysed by Cobas e 411 analyzer, a platform approved by Fetal Medicine Foundation (FMF) for prenatal screening assays. It is a fully automated analyzer that uses a patented ElectroChemiLuminescence (ECL) technology for immunoassay analysis.
Conditions & Symptoms
Routine screening for aneuploidy, history of a child or fetus with chromosomal aneuploidy such as Down syndrome, Edward syndrome, Patau Syndrome, Turner Syndrome etc, Ultrasound soft markers for fetal aneuploidy
Additional Information
GeneTech pioneered genetic testing in India in 1998 and has the most comprehensive range of tests using technologies.
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Our genetic counselling services empower patients and families by providing expert guidance on genetic conditions, their risks, and inheritance patterns. Our counsellors assess family medical histories to identify potential genetic risks and explain the benefits and limitations of genetic testing.
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Amniotic fluid is a clear, slightly yellowish liquid that surrounds the unborn baby (fetus) during pregnancy Amniocentesis is an ultrasound guided sterile proceedure performed by experienced radiologits to retrive 20-30ml of the amniotic fluid each from two dichorionic and diamniotic sacs. The fluid which contains fetal cells is used in the genetic lab to test for genetic abnormalities. It is done between 16-22 weeks of gestation. Amniocentesis proceedure is done at our central laboratory in Hyderabad. Prior appointment required. Call 9848041127 for details
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Test CatalogueDouble Marker Screening with Preeclampsia.

Full Body Checkup - Essential in Hyderabad

Unlock insights into your health, ancestry, or future risks with our advanced genetic testing. Backed by cutting-edge science and expert guidance, Genetech helps you make informed decisions—personalized to your DNA.

₹1599
₹2599
76% OFF
2 weeks
Schedule test now

Double Marker Screening with Preeclampsia.

First trimester maternal serum based double marker test is done at 11-13 wks of gestation. Down Syndrome and other common aneuploidy risk is calculated by testing two biochemical markers PAPP-A, beta-hCG and PLGF along with ultrasound markers such as NT/CRL and nasal bone.

3500
₹2599
76% OFF
3 days
Schedule test now
Sample collection and transportation
Sample Collection: 3ml Peripheral Blood in PURPLE TOP (EDTA) Vacutainer Transport within 48 hrs at room temperature
Download Brochure
Alternate Names
First trimester screening with preeclampsia, FTS with preeclampsis, Double marker testwith preeclampsia, FTS + PLGF, Double marker with Placental Growth Factor
Specialities
ObGyn, IVF, Fetal Medicine
Technology
The biochemical markers PAPP-A, beta-hCG and PLGF are analysed by Cobas e 411 analyzer, a platform approved by Fetal Medicine Foundation (FMF) for prenatal screening assays. It is a fully automated analyzer that uses a patented ElectroChemiLuminescence (ECL) technology for immunoassay analysis.
Conditions & Symptoms
Routine screening for aneuploidy, history of a child or fetus with chromosomal aneuploidy such as Down syndrome, Edward syndrome, Patau Syndrome, Turner Syndrome etc, Ultrasound soft markers for fetal aneuploidy
Related Tests
Genetic Counselling
Our genetic counselling services empower patients and families by providing expert guidance on genetic conditions, their risks, and inheritance patterns. Our counsellors assess family medical histories to identify potential genetic risks and explain the benefits and limitations of genetic testing.
750
2 weeks
Book now
Amniocentesis
Amniotic fluid is a clear, slightly yellowish liquid that surrounds the unborn baby (fetus) during pregnancy. Amniocentesis is an ultrasound guided sterile proceedure performed by experienced radiologits to retrive 20-30ml of the amniotic fluid from the womb. The fluid which contains fetal cells is used in the genetic lab to test for genetic abnormalities. It is done between 16-22 weeks of gestation. Amniocentesis proceedure is done at our central laboratory in Hyderabad. Prior appointment required. Call 9848041127 for details
7500
2 weeks
Book now
CVS Karyotyping
Karyotyping is a test performed on Chorionic Villi Sample (CVS) to identify fetal chromosomal numerical abnormalities (aneuploidy) and structural rearrangements such as inversions, insertions, translocations etc in the fetus.
8000
2 weeks
Book now

Frequently asked questions

What is Genetic Testing?
What are the uses of Genetic Testing?
What are the types of Genetic testing?
Are all genetic disorders hereditary?
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GeneTech is India’s leading genetics testing laboratory with the most comprehensive directory of genetic tests. We were established in Hyderabad in 1998, and have operations all over India.
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Book Counselling

GeneTech can provide online or offline counseling to patients in various languages. Some counseling sessions may require presence of a junior or on-duty physician for local language assistance.
Book counseling in advance. The date and time requested on this form are not confirmed until our Service Coordinator calls you to inform the appointment date and time, and payment for counseling is done.
Call +91-98480-41127 for any additional information or directions to pour branches or head-office.
GeneTech can provide online or offline counseling to patients in various languages. Some counseling sessions may require presence of a junior or on-duty physician for local language assistance.
Book counseling in advance. The date and time requested on this form are not confirmed until our Service Coordinator calls you to inform the appointment date and time, and payment for counseling is done.
Call +91-98480-41127 for any additional information or directions to pour branches or head-office.

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