Short Description

Microarray 60K (Peripheral Blood/Cord Blood/Fetal Blood) + Karyotyping is performed using Microarray [Agilent]+ Cell Culture methodology. Sample that have to be given is Peripheral blood in EDTA & Heparinised vacutainer (3 ml each) for this test. You can expect results in 7-9 days

PreTest Information

Microarray 60K (Peripheral Blood/Cord Blood/Fetal Blood) + Karyotyping 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

Microarray 60K (Peripheral Blood/Cord Blood/Fetal Blood) + Karyotyping Cost INR:22500 Symptoms Diagnosis

Microarray 60K is a genetic test that can analyze a person's DNA to detect any genetic variations or abnormalities. It is a type of molecular testing that can identify genomic changes that cause a range of genetic disorders. The test is performed on peripheral blood, cord blood, or fetal blood samples and is often used to diagnose chromosomal abnormalities and genetic disorders.

What is Karyotyping?

Karyotyping is a laboratory test that examines a person's chromosomes to detect any abnormalities. The test involves staining and examining chromosomes under a microscope to identify any changes in their number, structure, or size. Karyotyping can detect chromosomal abnormalities such as Down syndrome, Turner syndrome, and Klinefelter syndrome.

Why is Microarray 60K and Karyotyping performed?

Microarray 60K and Karyotyping are performed to diagnose genetic disorders and chromosomal abnormalities. The test is recommended for individuals who have symptoms of a genetic disorder, have a family history of a genetic disorder, or have had a previous pregnancy with a chromosomal abnormality. The test can also be performed during pregnancy to detect any chromosomal abnormalities in the fetus.

What are the symptoms of genetic disorders?

The symptoms of genetic disorders can vary depending on the type of disorder. However, some common symptoms of genetic disorders include developmental delays, intellectual disabilities, physical abnormalities, and growth problems. Other symptoms may include seizures, hearing loss, vision problems, and behavioral issues.

How is Microarray 60K and Karyotyping performed?

Microarray 60K and Karyotyping are performed by taking a blood sample from the patient. The blood sample is then sent to a laboratory for analysis. In the laboratory, the DNA is extracted from the blood sample and analyzed using specialized equipment. Microarray 60K analyzes the entire genome for genetic variations, while Karyotyping examines the chromosomes for any abnormalities.

What is the cost of Microarray 60K and Karyotyping?

The cost of Microarray 60K and Karyotyping in India is approximately INR 22,500. However, the cost may vary depending on the laboratory and the location.

Conclusion

Microarray 60K and Karyotyping are important genetic tests that can help diagnose genetic disorders and chromosomal abnormalities. The tests are performed on peripheral blood, cord blood, or fetal blood samples and are often recommended for individuals who have symptoms of a genetic disorder, have a family history of a genetic disorder, or have had a previous pregnancy with a chromosomal abnormality. The cost of the test in India is approximately INR 22,500, and the test can be performed in specialized laboratories.

If you are concerned about your genetic health or have symptoms of a genetic disorder, it is recommended that you consult a genetic counselor or a healthcare provider. They can help you understand the test results and provide you with appropriate treatment options.

For more information about Microarray 60K and Karyotyping, you can contact DNA Labs India, a leading provider of genetic testing services in India.