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Karyotyping for Genetic Disorder Test Cost & Procedure

Karyotyping for Genetic Disorder

Karyotyping For Genetic Disorder

Book Karyotyping For Genetic Disorder Appointment Online at the best price in Delhi/NCR from Ganesh Diagnostic. NABL & NABH Accredited Diagnostic centre in Delhi offering a wide range of Radiology & Pathology tests. Get Free Ambulance & Free Sample collection from Home. 24 Hour Open.

₹ 3850 ₹ 3080

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DNA, which is carried by genes, carries information that regulates how your body functions and how you look.

Why does the karyotype test examine your cells' chromosomes?

 Health, growth, and normal development can be severely hampered by having too many or too few chromosomes. (missing X chromosome).

Check for chromosome structural alterations, such as additional, damaged, or missing sections. Depending on which chromosome is impacted, these mutations could result in a wide range of issues. Yet, certain chromosomal abnormalities don't lead to issues. A few chromosomal issues exist from birth. Certain cells can experience chromosomal issues even after birth. Certain cancers can develop as a result of these issues. Alternative terms include cytogenetic analysis, chromosome research, genetic testing, and chromosome testing.

What does it serve?

A karyotype test searches for uncommon chromosomal abnormalities. It could be applied to:

  • Check your chromosomes and/or those of your family members if you:
  • posses a hereditary condition that runs in your family
  • possess signs that could be related to a genetic condition

Check for chromosomal issues in a foetus.

  • Check to see if aberrant chromosomes are the source of the issue. bringing up a child, including:
    • Infertility in either men or women
    • If you have lost two or more pregnancies before 20 weeks, you have miscarriages.
    • Stillbirth
    • assist in making a diagnosis and/or treatment decisions

Why is a karyotype test necessary?

If any of the following applies to you: You're expecting a child or planning a pregnancy:

can determine if you, your spouse, or both of you have faulty chromosomes that could be passed on to a child. to perform a genetic abnormality screening on your unborn child, particularly if the infant is at high risk for issues. If the parent is 35 years of age or older and pregnant, the risk may be considerable. Although the incidence of genetic birth abnormalities is low overall, it rises after age 35.

This may be instructed to support the diagnosis and therapy of illnesses like:

  • Leukemia

Lymphoma

  • several myelomas

Anaemia

How does a karyotype test work?

For karyotype assays, this sample is most frequently utilized. 

  • Blood is withdrawn with a needle

To collect a sample of cells, a medical expert will place a swab inside your mouth and rub it around the inside of your cheek.

  • a test for bone marrow. If you have a specific form of cancer or blood problem, this test might be used on you. Within the bones is a soft, spongy tissue called marrow. The rear of the hip bone is where the majority of bone marrow samples are collected.

Test Type Karyotyping For Genetic Disorder
Includes

Karyotyping for Genetic Disorder (Pathology Test)

Preparation
Reporting

Within 24 hours*

Test Price ₹ 3080 ₹ 3850
Frequently Asked Questions
FAQ

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