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Fetal Blood for Karyotyping Test

1,000 د.إ

-17%

**Fetal Blood for Karyotyping Test at DNA Labs UAE**

The Fetal Blood for Karyotyping Test is a critical prenatal examination offered at DNA Labs UAE, designed to analyze the chromosomes of a fetus to identify any genetic abnormalities. This test is particularly important for expecting parents concerned about the genetic health of their unborn child, as it can detect conditions such as Down syndrome, Edwards syndrome, Patau syndrome, and other chromosomal anomalies.

Performed by drawing a small sample of the fetus’s blood, this procedure is carefully conducted to ensure both the mother’s and the fetus’s safety. The extracted fetal blood is then subjected to detailed chromosomal analysis, where the karyotype – the complete set of chromosomes – is examined for any irregularities in number, structure, or arrangement.

The cost of the Fetal Blood for Karyotyping Test at DNA Labs UAE is set at 1000 AED. This investment covers the expertise of the laboratory’s genetic specialists, the use of advanced diagnostic technology, and a comprehensive report that provides expectant parents with crucial information about their fetus’s genetic health. With this test, families can make informed decisions and prepare for any necessary medical interventions or support.

DNA Labs UAE is renowned for its commitment to accuracy, confidentiality, and support throughout the testing process, making it a trusted choice for families seeking peace of mind during pregnancy.

Home  Sample collection service available

  • 100% accuaret Test Results
  • Ranked as Most trusted Genetic DNA Lab
  • This test is not intended for medical diagnosis or treatment
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Fetal Blood for Karyotyping Test

Test Name: Fetal blood for Karyotyping Test

Components: Sodium Heparin Vacutainer (2ml)

Price: 1000.0 AED

Sample Condition: Peripheral blood/Fetal blood

Report Delivery: 7-9 days

Method: Cell culture

Test Type: Genetics

Doctor: Gynecologist

Test Department: Pre Test Information

Fetal blood for Karyotyping can be done with a Doctor’s prescription. Prescription is not applicable for surgery and pregnancy cases or people planning to travel abroad.

Test Details

Fetal blood can be collected for karyotyping, which is a test that examines the chromosomes of an individual to detect any abnormalities or genetic disorders. Karyotyping can provide valuable information about the baby’s genetic makeup and help diagnose conditions such as Down syndrome, Turner syndrome, or certain chromosomal abnormalities.

To collect fetal blood for karyotyping, a procedure called cordocentesis, or percutaneous umbilical blood sampling (PUBS), is performed. This procedure involves inserting a thin needle into the umbilical cord under ultrasound guidance to withdraw a small sample of fetal blood. The blood sample is then sent to a laboratory for karyotyping analysis.

Cordocentesis is typically performed in the second or third trimester of pregnancy when there is a specific reason to assess the baby’s chromosomes. It is considered an invasive procedure and carries a small risk of complications, including bleeding or infection. Therefore, it is usually reserved for cases where there is a suspected or known genetic condition that requires further investigation.

Overall, fetal blood collection for karyotyping can provide valuable information about the baby’s chromosomes and help guide medical management and counseling for families. However, it is important to discuss the risks and benefits of this procedure with a healthcare provider to make an informed decision.

Test Name Fetal blood for Karyotyping Test
Components Sodium Heparin Vacutainer (2ml)
Price 1000.0 AED
Sample Condition Peripheral blood\/Fetal blood
Report Delivery 7-9 days
Method Cell culture
Test type Genetics
Doctor Gynecologist
Test Department:
Pre Test Information Fetal blood for Karyotyping can be done with a Doctors prescription. Prescription is not applicable for surgery and pregnancy cases or people planing to travel abroad.
Test Details

Fetal blood can be collected for karyotyping, which is a test that examines the chromosomes of an individual to detect any abnormalities or genetic disorders. Karyotyping can provide valuable information about the baby’s genetic makeup and help diagnose conditions such as Down syndrome, Turner syndrome, or certain chromosomal abnormalities.

To collect fetal blood for karyotyping, a procedure called cordocentesis, or percutaneous umbilical blood sampling (PUBS), is performed. This procedure involves inserting a thin needle into the umbilical cord under ultrasound guidance to withdraw a small sample of fetal blood. The blood sample is then sent to a laboratory for karyotyping analysis.

Cordocentesis is typically performed in the second or third trimester of pregnancy when there is a specific reason to assess the baby’s chromosomes. It is considered an invasive procedure and carries a small risk of complications, including bleeding or infection. Therefore, it is usually reserved for cases where there is a suspected or known genetic condition that requires further investigation.

Overall, fetal blood collection for karyotyping can provide valuable information about the baby’s chromosomes and help guide medical management and counseling for families. However, it is important to discuss the risks and benefits of this procedure with a healthcare provider to make an informed decision.

SKU: TEST-5755 Category:

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