High Density 750K Chromosomal Array- Price, Normal Range | Sprint Diagnostics Hyderabad

Patient Preparing : No specific preparation, such as fasting, is needed for this test.

₹ 25000


The Chromosomal Array - Peripheral Blood: High Density 750K is a sophisticated genetic test. It provides an even more detailed look at an individual's genetic makeup by analyzing over 750,000 unique genetic markers. This comprehensive examination helps identify minor chromosomal imbalances that could contribute to various health concerns, including intellectual disabilities, developmental delays, and physical abnormalities.

Test Name Chromosomal Array - Peripheral Blood: High Density 750K
Sample Type Blood
Preparations Required No specific preparation, such as fasting, is needed for this test.
Report Time 12 days
Price in Hyderabad ₹ 25000

What is a Chromosomal Array - Peripheral Blood: High Density 750K test?

This is a genetic test that analyzes over 750,000 genetic markers in a blood sample. It can identify minor chromosomal imbalances which could be associated with various genetic disorders.

Why would I need a High Density 750K Chromosomal Array test?

This test is often recommended for individuals with developmental delays, intellectual disabilities, physical abnormalities, or unexplained miscarriages that cannot be diagnosed through conventional genetic tests.

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How is the Chromosomal Array - Peripheral Blood: High Density 750K test performed?

Your doctor will draw a blood sample from a vein in your arm, which will then be sent to a laboratory. The lab will then use specialized techniques to analyze the sample for chromosomal imbalances.

When should I get this test?

Your doctor may recommend this test if you or your child exhibits symptoms suggesting a genetic disorder, such as developmental delays, intellectual disability, or unusual physical features. It may also be used in cases of unexplained recurrent miscarriages.

What do the results of the High Density 750K Chromosomal Array test mean?

The results can detect minor imbalances in the chromosomes. An abnormal result might indicate the presence of a genetic disorder, but interpretation of the results is complex and requires the expertise of a genetic specialist.

What are the risks of the High Density 750K Chromosomal Array test?

The risks are mainly associated with the blood draw, which may cause slight discomfort, bruising, or bleeding at the injection site.

How should I prepare for this test?

No specific preparation, such as fasting, is needed for this test.

Can other factors affect my test results?

No, the results of a chromosomal array test are not typically influenced by lifestyle or environmental factors.

What kind of doctor should I see if my Chromosomal Array test results are abnormal?

In the event of abnormal results, you should consult a genetic counselor or a medical geneticist. These specialists can help interpret the test results and discuss the potential implications for you and your family.

What is the treatment if my Chromosomal Array test results are abnormal?

The specific treatment will depend on the genetic disorder identified by the test. It may range from medical interventions to supportive care, such as speech therapy, physical therapy, or educational support.

Is fasting required for this test?

No, fasting is not required for this test.

What are the normal values for a Chromosomal Array test?

A normal result indicates that there are no significant chromosomal imbalances detected.

How often should I get tested?

This test is usually a one-time procedure ordered based on specific clinical indications.

What precautions should I take after the test?

There are no specific precautions necessary after the test.

Is the test painful?

The test involves a blood draw, which can cause mild discomfort but is generally not considered painful.

How long does it take to get the results?

Results are typically available within 1-2 weeks.

The Chromosomal Array - Peripheral Blood: High Density 750K test offers a comprehensive analysis of an individual's genetic makeup. By identifying minor chromosomal imbalances, the test can provide valuable insights into the causes of unexplained symptoms or conditions, potentially guiding treatment strategies and informing family planning decisions. As with any medical procedure, it's crucial to discuss any concerns or questions with your doctor.

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