Short Description

This assay determines the chromosomal status of the fetus including Numerical and structural abnormalities. Mosaicism can be ruled out in samples drawn after 15 weeks of gestation.

PreTest Information

Test is recommended between 15-20 weeks of gestation. Duly filled Chromosome & FISH Analysis Requisition form (Form 17) & Consent form (Form 18) for Prenatal Genetic Testing is mandatory.

Detail Description

Chromosome Analysis Amniotic Fluid Test: Cost, Symptoms, and Diagnosis

Chromosome analysis amniotic fluid test is a medical procedure that involves analyzing the chromosomes of a developing fetus. This test is usually carried out during the second trimester of pregnancy and is used to detect any chromosomal abnormalities that may be present in the fetus. In this blog, we will discuss the cost, symptoms, and diagnosis of chromosome analysis amniotic fluid test.

Cost of Chromosome Analysis Amniotic Fluid Test

The cost of the chromosome analysis amniotic fluid test in India ranges from INR 13,000 to INR 20,000. The cost may vary depending on the location of the laboratory, the expertise of the medical professional, and the complexity of the test. It is important to note that this test is not covered by insurance in most cases and the cost has to be borne by the patient.

Symptoms that may require Chromosome Analysis Amniotic Fluid Test

There are several symptoms that may indicate the need for chromosome analysis amniotic fluid test. These include:

• Advanced maternal age (35 years or older)
• History of chromosomal abnormalities in previous pregnancies
• Fetal abnormalities detected during ultrasound
• Family history of genetic disorders

If any of the above symptoms are present, it is important to consult a medical professional who can recommend the appropriate tests.

Diagnosis of Chromosome Analysis Amniotic Fluid Test

The diagnosis of chromosome analysis amniotic fluid test involves the following steps:

• The medical professional will first collect a sample of amniotic fluid from the uterus using a needle.
• The sample will then be sent to a laboratory where the chromosomes of the fetus will be analyzed.
• The results of the test will be shared with the medical professional who will then discuss the findings with the patient.

It is important to note that chromosome analysis amniotic fluid test is an invasive procedure and carries a small risk of miscarriage. Therefore, this test should only be carried out if it is absolutely necessary.

Conclusion

Chromosome analysis amniotic fluid test is an important medical procedure that can help detect chromosomal abnormalities in a developing fetus. It is important to consult a medical professional if any symptoms are present that may indicate the need for this test. While the cost of the test may vary, it is important to remember that this test is not covered by insurance in most cases and the cost has to be borne by the patient.

Overall, chromosome analysis amniotic fluid test can help parents make informed decisions about their pregnancy and ensure the best possible outcome for their child.

For more information about chromosome analysis amniotic fluid test, please contact DNA Labs India.