Amniotic Fluid for Karyotyping

Amniotic Fluid for Karyotyping is a prenatal test that analyzes the chromosomes in the amniotic fluid to detect genetic abnormalities. This test measures various health markers to assess the risk of chromosomal disorders in the fetus. It is typically recommended between 15-20 weeks of gestation.

Quick Summary

Amniotic Fluid for Karyotyping Price AED 2000, Sample 20 mL (15 mL min.) Amniotic fluid in a sterile screw-capped container. Sample to be collected under strict aseptic precautions. Ship refrigerated immediately. DO NOT FREEZE. Specimen must reach within 48 hours. Test is recommended between 15-20 weeks of gestation. Duly filled Prenatal Genetic Testing Consent Form is mandatory. It is recommended to discard the initial 2-3 mL of aspirate, since this "first draw" may contain some maternal cells trapped within the needle during insertion., Results in 10 - 15 Days. Home collection available.

Test Overview

Result Time

10 - 15 Days

Sample Type

20 mL (15 mL min.) Amniotic fluid in a sterile screw-capped container. Sample to be collected under strict aseptic precautions. Ship refrigerated immediately. DO NOT FREEZE. Specimen must reach within 48 hours. Test is recommended between 15-20 weeks of gestation. Duly filled Prenatal Genetic Testing Consent Form is mandatory. It is recommended to discard the initial 2-3 mL of aspirate, since this "first draw" may contain some maternal cells trapped within the needle during insertion.

How to Prepare

To prepare for the test, collect 20 mL (15 mL minimum) of amniotic fluid in a sterile screw-capped container under strict aseptic precautions. The sample must be shipped refrigerated immediately and should not be frozen. It is essential that the specimen reaches the testing facility within 48 hours. The test is recommended between 15-20 weeks of gestation, and a duly filled Prenatal Genetic Testing Consent Form is mandatory. Discard the initial 2-3 mL of aspirate, as this 'first draw' may contain maternal cells trapped during needle insertion.

Why You Need This Test

This test is crucial for identifying potential genetic disorders in the fetus, allowing for early intervention and informed decision-making. It is particularly recommended for expectant mothers who are at increased risk for chromosomal abnormalities due to age or family history.

Clinical Significance

The test plays a vital role in prenatal screening for chromosomal abnormalities.

At a Glance

Quick Facts

• Price AED 2000
• Sample 20 mL (15 mL min.) Amniotic fluid in a sterile screw-capped container. Sample to be collected under strict aseptic precautions. Ship refrigerated immediately. DO NOT FREEZE. Specimen must reach within 48 hours. Test is recommended between 15-20 weeks of gestation. Duly filled Prenatal Genetic Testing Consent Form is mandatory. It is recommended to discard the initial 2-3 mL of aspirate, since this "first draw" may contain some maternal cells trapped within the needle during insertion.
• Results in 10 - 15 Days
• Fasting Not required

What It Measures

Amniotic Fluid for Karyotyping is a prenatal test that analyzes the chromosomes in the amniotic fluid to detect genetic ...

Frequently Asked Questions

What does this test measure?

This test measures the chromosomes in the amniotic fluid to detect any genetic abnormalities that may affect the fetus. It provides valuable information regarding the risk of chromosomal disorders.

Who should take this test?

Expectant mothers who are between 15-20 weeks of gestation and have concerns about genetic disorders or have a family history of chromosomal abnormalities should consider this test. It is also recommended for women of advanced maternal age.

How do I prepare for this test?

Preparation involves collecting 20 mL (15 mL minimum) of amniotic fluid in a sterile screw-capped container under strict aseptic conditions. The sample must be shipped refrigerated immediately and should not be frozen. Ensure the specimen arrives within 48 hours and complete the Prenatal Genetic Testing Consent Form.

What do the results mean?

Results will indicate whether any chromosomal abnormalities are present. Abnormal results may suggest the need for further testing or counseling regarding potential genetic conditions.

How long until I get my results?

Results are typically available within 10 to 15 days. They will be delivered through the specified communication method provided during the testing process.

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