Peripheral blood for High resolution Couple Karyotyping Cost 7600 Rs

Peripheral blood for High resolution Couple Karyotyping

Peripheral blood for High resolution Couple Karyotyping

Disease: Genetics

Method: Cell culture

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Sample Types
  • Blood Sodium Heparin

7,600.00/- Rs ₹11,200.0032% off

  • Results in : 10-12 days
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Peripheral blood for High resolution Couple Karyotyping Cost 7600 Rs

Test Name Peripheral blood for High resolution Couple Karyotyping
Test type Gynecologist
Pre-test Information Peripheral blood for High resolution karyotyping (COUPLE) can be done with a Doctor’s prescription. Prescription is not applicable for surgery and pregnancy cases or people planing to travel abroad.
Report Delivery 10-12 days
Components Sodium Heparin Vacutainer (2ml)
Price ₹ 7600
Method Cell culture

Peripheral blood for High resolution Couple Karyotyping Details

Short Description

Peripheral blood for High resolution karyotyping (COUPLE) is performed using Cell culture methodology. Sample that have to be given is Peripheral blood in Sodium Heparin Vacutainer (2ml) for this test. You can expect results in 7-9 days

Test Specifications

  • Speciality: Gynecologist

  • Components: Sodium Heparin Vacutainer (2ml)

  • Department:

  • Shipping Stability: Ambient

PreTest Information

Peripheral blood for High resolution karyotyping (COUPLE) can be done with a Doctor’s prescription. Prescription is not applicable for surgery and pregnancy cases or people planing to travel abroad.

Detail Description

What is Karyotyping?

Chromosome analysis or karyotyping is a test that evaluates the number and structure of a person's chromosomes in order to detect abnormalities. A karyotype may be used to diagnose genetic diseases, some birth defects, such as Down syndrome, or leukaemia and lymphoma.

What Are Karyotype Tests?

Karyotype tests take a close look at the chromosomes inside your cells to see if anything about them is unusual. They're often done during pregnancy to spot problems with the baby. This type of procedure is also referred to as genetic or chromosome testing, or cytogenetic analysis.

Most women get results that are within the normal range and don't need any further tests. But if any of your screening tests show signs of a problem, the doctor will offer you follow-up tests so you can find out for sure whether your growing baby has any genetic or chromosomal problems.

Uses for Karyotype Tests

Humans have 46 chromosomes. Babies inherit 23 from their mom and 23 from their dad.

Sometimes, babies have an extra chromosome, a missing chromosome, or an abnormal chromosome. Karyotype tests will see if any of these have happened with your baby. The most common things doctors look for with karyotype tests include:

  • Down syndrome (trisomy 21). A baby has an extra, or third, chromosome 21. This affects how the baby looks and learns.
  • Edwards syndrome (trisomy 18). A baby has an extra 18th chromosome. These babies usually have many problems, and most don't live longer than a year.
  • Patau syndrome (trisomy 13). A baby has an extra 13th chromosome. These babies usually have heart problems and severe mental impairment. Most won't live more than a year.
  • Klinefelter syndrome. A boy baby has an extra X chromosome (XXY). They may go through puberty at a slower pace, and may not be able to have children.
  • Turner syndrome. A girl baby has a missing or damaged X chromosome. It causes heart problems, neck problems, and short height.

What is the cost of Karyotyping Test?

Karyotyping for Single costs 4000 Rs

What is the reporting time for Karyotyping Test?

Karyotyping takes 8-10 working days

What is being tested?

Chromosome analysis or karyotyping is a test that evaluates the number and structure of a person's chromosomes in order to detect abnormalities. Chromosomes are thread-like structures within each cell nucleus and contain the body's genetic blueprint. Each chromosome contains thousands of genes in specific locations.

Chromosome analysis or karyotyping is a test that evaluates the number and structure of a person's chromosomes in order to detect abnormalities. Chromosomes are thread-like structures within each cell nucleus and contain the body's genetic blueprint.

Each chromosome contains thousands of genes in specific locations. These genes are responsible for a person's inherited physical characteristics and they have a profound impact on growth, development, and function.

Karyotype Test Results

When the lab sends your results back, they've looked at your baby's chromosomes, so the results are definite: Either your baby has a genetic problem or they don't. This is different from earlier screening tests, which could only say there's a high or low chance of a problem. Your doctor will discuss the test results with you.

 

 

 

 

 

Frequently Asked Questions

  • What is the cost of Peripheral blood for High resolution Couple Karyotyping?

    Cost of Peripheral blood for High resolution Couple Karyotyping is 7600 Rs

  • Are there any risks with a karyotype test?

    There are no significant risks with a blood test, but you might experience:

    Light bleeding where the needle went into your vein.

    Soreness on the inside of your arm.

  • How many days for reports to come?

    Reports will take 8-10 working days

  • How the Test Is Done?

    For infertile couples, the test is usually done via a blood draw, from both the male and female partners. The blood samples are then processed in a lab. 

  • Should everyone have this testing done?

    Chromosome analysis is frequently performed, but it is not indicated as a general screening test. The majority of people will never need to have one done.

  • What do karyotype test results mean?

    Abnormal karyotype test results could mean that you or your baby have unusual chromosomes. 

  • What is a karyotype test?

    A karyotype test uses blood or body fluids to analyze your chromosomes. Chromosomes are the parts of our cells that contain genes, which consist of DNA. You inherit genes from your parents. Genes determine your traits, such as your eye and skin colour.

  • What is the cost of Karyotyping test?

    Karyotyping test cost 7600

  • When to go for the test?

    Chromosome analysis may be ordered when a fetus is suspected of having a chromosomal abnormality when an infant has congenital abnormalities, when a woman experiences miscarriages or infertility, and when an adult shows signs of a genetic disorder. 

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