Short Description

Mucopolysaccharidoses are autosomal recessive disorders with the exception of MPS II which follows an X-linked inheritance pattern. This assay detects specific sulphate with qualitative analysis of their relative amounts. It is also useful for monitoring effectiveness of enzyme replacement therapy.

PreTest Information

Sample should be taken after 16 weeks gestation. Duly filled Prenatal genetic testing consent form (Form 18) is mandatory. Sample to be dispatched with prior appointment.

Detail Description

PRENATAL DIAGNOSIS PANEL 2 AMNIOTIC FLUID Test: Symptoms, Diagnosis, and Cost

When a woman is pregnant, she wants to ensure the health of her baby. One of the ways to do that is through prenatal testing. Prenatal diagnosis panel 2 amniotic fluid test is one such test that can help detect any genetic abnormalities in the fetus. In this blog, we will discuss the symptoms, diagnosis, and cost of the prenatal diagnosis panel 2 amniotic fluid test.

Symptoms

There are no specific symptoms that indicate the need for a prenatal diagnosis panel 2 amniotic fluid test. However, it is usually recommended for women who are at an increased risk of having a baby with a genetic disorder. Some of the factors that may increase the risk include:

• Advanced maternal age (35 years or older)
• Family history of genetic disorders
• Previous child with a genetic disorder
• Pregnancy with multiples

If any of the above factors are present, then the doctor may recommend the prenatal diagnosis panel 2 amniotic fluid test.

Diagnosis

The prenatal diagnosis panel 2 amniotic fluid test is a type of prenatal genetic testing. It involves analyzing the amniotic fluid for any genetic abnormalities. The test is usually performed between 15 and 20 weeks of pregnancy.

The test involves inserting a thin needle through the abdomen into the uterus to collect a small amount of amniotic fluid. The fluid is then sent to a laboratory for analysis. The results of the test can take several weeks to come back.

The test can detect a variety of genetic disorders, including Down syndrome, cystic fibrosis, and sickle cell disease. It can also detect neural tube defects, such as spina bifida.

Cost

The cost of the prenatal diagnosis panel 2 amniotic fluid test in India is around INR 5850. However, the cost may vary depending on the location and the laboratory performing the test.

It is important to note that the cost of the test may not be covered by insurance. It is important to check with your insurance provider before undergoing the test.

Conclusion

The prenatal diagnosis panel 2 amniotic fluid test is an important tool in detecting genetic abnormalities in the fetus. It is usually recommended for women who are at an increased risk of having a baby with a genetic disorder. The test involves analyzing the amniotic fluid for any genetic abnormalities and can detect a variety of genetic disorders. The cost of the test may vary depending on the location and the laboratory performing the test. If you are pregnant and have any of the risk factors, it is important to talk to your doctor about the prenatal diagnosis panel 2 amniotic fluid test.