Bone Marrow Sample - Peripheral Blood - Price, Normal Range | Sprint Diagnostics Hyderabad

Patient Preparing : Inform your doctor of any medications or supplements you are taking. Follow any guidelines regarding food, drink, or medication consumption prior to the procedure.

₹ 750


Bone marrow is a soft, spongy tissue within bones that produces blood cells. Peripheral blood refers to blood that circulates throughout the body. Cytogenetics is a branch of genetics that studies the structure and function of cells, especially chromosomes. Bone Marrow Sample/Peripheral Blood Preservation for Cytogenetics is a critical diagnostic procedure that involves taking samples of bone marrow or peripheral blood and preserving them for cytogenetic analysis.

This process helps in the evaluation of genetic disorders, cancers, and various diseases affecting blood and bone marrow. The preservation of samples is crucial as it ensures that the cell structures stay intact for accurate analysis.

Test Name Bone Marrow Sample/Peripheral Blood Preservation for Cytogenetics
Sample Type Bone Marrow or Peripheral Blood
Preparations Required Inform your doctor of any medications or supplements you are taking. Follow any guidelines regarding food, drink, or medication consumption prior to the procedure.
Report Time 2 Days
Price in Hyderabad ₹ 750

Why is this test important?

This test is crucial for diagnosing and monitoring diseases and conditions that affect the blood and bone marrow, such as leukemia, lymphoma, and other genetic disorders. The analysis helps in understanding the genetic makeup of the cells, which is vital for targeted treatment plans.

How is a bone marrow sample collected?

A bone marrow sample is usually collected from the hip bone. The area is numbed with local anesthesia, and a needle is inserted into the bone to extract a small sample of bone marrow.

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How is a peripheral blood sample collected?

A peripheral blood sample is collected by drawing blood from a vein, usually in the arm. This is a standard blood draw procedure.

What is cytogenetic analysis?

Cytogenetic analysis involves examining the chromosomes in cells. This analysis can reveal genetic abnormalities that might cause various diseases, including cancers.

What are chromosomes?

Chromosomes are structures within cells that contain DNA. They are vital for the growth, development, and functioning of the body.

Is the procedure painful?

A peripheral blood draw is generally quick and may cause a brief stinging sensation. Bone marrow aspiration can be more uncomfortable, but local anesthesia is used to minimize pain.

What happens after the sample is collected?

Once collected, the sample is preserved and sent to a laboratory where cytogenetic analysis is performed. The cells are stained and examined under a microscope for any abnormalities in the chromosomes.

How should I prepare for the procedure?

Your doctor will provide specific instructions based on your health history. Generally, no significant preparation is needed for a blood draw. For bone marrow sampling, you might be asked to fast for a certain period before the procedure.

What do the results mean?

The results of the cytogenetic analysis can indicate the presence of genetic disorders, cancers, or other conditions affecting the blood and bone marrow. Your doctor will interpret the results and discuss the next steps or treatment options with you.

Are there any risks associated with these procedures?

Peripheral blood sampling is low risk. Bone marrow aspiration may have risks such as infection, bleeding, or reaction to anesthesia.

Why is preservation important?

Preservation of the sample is critical to maintaining the integrity of the cells, which ensures that the laboratory can accurately analyze the chromosomes.

What factors might affect the results?

Medications, underlying health conditions, and the quality of the sample preservation can affect the results.

How are the results used in treatment?

Results can guide decisions regarding treatment, including the choice of medications or therapies that target specific genetic abnormalities.

Can the results affect my family members?

Certain genetic disorders can be inherited. If you are diagnosed with a genetic disorder, it might be relevant information for family members.

Which doctor should I consult if my results are abnormal?

In case of abnormal results, you should consult a hematologist or a medical geneticist, depending on the condition diagnosed.

Understanding your genetic makeup, particularly how it affects your blood and bone marrow, is vital for targeted treatment and management of various conditions. This test provides insights into your chromosomes and any potential abnormalities. The results can be life-changing, as they may not only affect you but potentially your family as well. Consultation and open communication with your doctor are key components in understanding and utilizing these results for your health.

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