Chromosomal Karyotyping Test in HSR Layout, Bangalore

Chromosomal Karyotyping is a genetic test that analyzes the number and structure of chromosomes in a cell. It is used to diagnose genetic disorders, such as Down syndrome, and to understand the causes of infertility and miscarriage.

How Does Chromosomal Karyotyping Work?

The test is performed on cells, such as blood or skin cells, which are taken from the patient. The cells are then grown in a laboratory and treated with chemicals that make the chromosomes visible under a microscope. The chromosomes are then photographed and analyzed to identify any abnormalities.

What are the Benefits of Chromosomal Karyotyping?

Chromosomal karyotyping can provide important information about the genetic makeup of a patient, including the presence of genetic disorders and the cause of infertility or miscarriage. This information can be used to make informed decisions about treatment and can provide peace of mind for couples who are looking to start a family.

Who Should Consider Chromosomal Karyotyping?

If you or your partner have a family history of genetic disorders, have experienced infertility or recurrent miscarriages, or are at increased risk for these conditions, chromosomal karyotyping may be right for you. Consult with your doctor to determine if this test can help diagnose and treat your condition.

FAQ's on Chromosomal Karyotyping Treatment