Your Cart
Your cart is empty

Looks like you haven't added any test / checkup to your cart

Add Test / Checkup
User Sign In Health checkup offers
acetone-serum

Amniotic Fluid Karyotyping for Twins

Amniotic fluid karyotyping for twins is a prenatal diagnostic procedure used to analyze the chromosomes of the fetuses in a twin pregnancy. This is performed to detect chromosomal abnormalities such as Down syndrome, or other genetic disorders. The procedure involves extracting a small sample of amniotic fluid, which contains fetal cells, from the amniotic sacs of both fetuses. The chromosomes within the fetal cells are then analyzed for any abnormalities. This test is usually conducted between the 15th and 20th weeks of pregnancy.


  • Test NameAmniotic Fluid Karyotyping for Twins
  • Sample TypeAmniotic Fluid
  • Preparations RequiredThere are no specific preparations required for the patient prior to the procedure. However, it is advisable to wear loose and comfortable clothing to the appointment. Post-procedure, it is recommended to avoid strenuous activities for the rest of the day.
  • Report Time21 days

What is amniotic fluid karyotyping?

Amniotic fluid karyotyping is a procedure where a sample of amniotic fluid is collected from the womb during pregnancy, and the chromosomes in the cells found in the fluid are analyzed to detect any genetic or chromosomal abnormalities in the fetus.

Why is karyotyping for twins performed?

This test is performed for twins to detect if there are any genetic disorders or chromosomal abnormalities in either or both of the fetuses. It helps in identifying conditions such as Down syndrome, Edwards syndrome, or other genetic abnormalities that may affect the development of the babies.

Home Sample Collection Process

1
Book your convenient slot
Book your convenient slot
2
Sample Collection by Phlebotomist
Sample Collection by Phlebotomist
3
Reporting of the sample at lab
Reporting of the sample at lab
4
Download Reports
Download Reports
Frequently Asked Questions

The procedure, known as amniocentesis, involves inserting a thin needle through the abdomen into the uterus, and extracting a small amount of amniotic fluid from the sacs surrounding the fetuses. Ultrasound is used to guide the needle safely. The procedure is performed separately for each fetus in a twin pregnancy.

Amniotic fluid karyotyping is considered relatively safe but it is an invasive procedure and does carry a small risk of complications such as infection, leaking amniotic fluid, or miscarriage. The risks and benefits should be discussed with the doctor.

If the karyotyping shows that the chromosomes are normal, it is unlikely that the fetuses have chromosomal abnormalities. If an abnormality is detected, further testing and counseling will be recommended to understand the implications.

The results usually take between 14 to 21 days to be processed, as the cells need to be cultured and grown before the chromosomes can be analyzed.

If a chromosomal abnormality is detected, genetic counseling will be provided to the parents to discuss the findings, potential implications, and options moving forward.

Some women report feeling mild discomfort or cramping during the procedure. There might be slight soreness at the needle insertion site afterward.

Yes, since this test analyzes the chromosomes, it can determine the sex of each fetus.

No, this test is not mandatory. It is usually offered when there is a family history of genetic disorders, abnormal ultrasound findings, or if the mother is of advanced maternal age.

Yes, there are alternative tests such as chorionic villus sampling and non-invasive prenatal testing that can also provide information on chromosomal abnormalities.

It is normal to experience some mild cramping or discomfort after the procedure. It’s advised to avoid strenuous activities and rest for the remainder of the day.

Yes, it is generally recommended to avoid strenuous physical activity for at least 24 hours following the procedure.

If chromosomal abnormalities are detected, it is important to consult a genetic counselor or a perinatologist (a doctor specialized in high-risk pregnancies) to discuss the results and understand the options.

No, amniotic fluid karyotyping primarily detects chromosomal abnormalities. There are other genetic disorders caused by mutations in single genes that are not detected by this test.

The amniotic fluid karyotyping for twins is a valuable procedure that can provide critical information about the genetic health of fetuses in a twin pregnancy. However, it is important to weigh the benefits against the risks, and make an informed decision in consultation with a healthcare professional. Whether you opt for this test or not, it’s important to engage in regular prenatal care to support the healthiest outcome for your pregnancy.

Amniotic Fluid Karyotyping for Twins
₹ 16000
Schedule Test in Your Available Time
Locations Near You in Hyderabad
  • 4KM from Madhapur
  • 3KM from Banjara Hills
  • 1.9KM from Yusufguda
  • 3KM from Madhura Nagar
  • 5KM from Shaikpet