Smart Cytogenetics 6 Test, Price, Normal Range | Sprint Diagnostics Hyderabad

Patient Preparing : No special preparation is necessary for this test.

₹ 22250


Smart Cytogenetics 6 is an advanced diagnostic test that combines two powerful techniques - Karyotyping and Fluorescence In Situ Hybridization (FISH) to analyze six specific genetic markers in a blood sample. Karyotyping is a laboratory procedure that provides a visual profile of an individual’s chromosomes. It is instrumental in identifying abnormalities in the number and structure of chromosomes. On the other hand, FISH is a technique that uses fluorescent probes to bind to specific DNA sequences, allowing for the detection of genetic mutations and abnormalities. By examining six genetic markers, Smart Cytogenetics 6 offers a more comprehensive analysis of an individual's genetic material. This is particularly useful in the diagnosis of complex genetic disorders and in certain cancer types.

Test Name Smart Cytogenetics 6: Karyotyping and FISH for Six Markers
Sample Type Blood/ bone marrow
Preparations Required No special preparation is necessary for this test.
Report Time 12 Days for Karyotype & 5 Days for FISH
Price in Hyderabad ₹ 22250

What is the importance of the Smart Cytogenetics 6 test?

Smart Cytogenetics 6 is essential for identifying chromosomal abnormalities and detecting specific genetic mutations. Its capability to analyze six markers offers a broader scope of information, which can be critical in diagnosing and managing various genetic disorders and cancers.

Do I need to fast before taking the Smart Cytogenetics 6 test?

No, fasting is not required before undergoing the Smart Cytogenetics 6 test.

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What specific preparations are needed before the test?

There are no special preparations necessary for this test. However, it’s advisable to inform your doctor about any medications or supplements you are taking.

Who should consider taking the Smart Cytogenetics 6 test?

Individuals who are suspected of having genetic disorders, as well as patients with certain types of cancers, especially those where multiple genetic alterations are suspected, might be advised to undergo this test.

What kind of information does Smart Cytogenetics 6 provide?

Smart Cytogenetics 6 provides detailed information regarding the structure and number of chromosomes. It can also detect specific genetic abnormalities by analyzing six different markers.

How often should this test be performed?

The frequency of the test depends on the patient’s condition and the recommendations of the doctor. In cases of chronic disorders or cancers, it may be performed periodically for monitoring purposes.

What do normal values indicate?

Normal values typically indicate a standard number and structure of chromosomes. However, results can vary, so it’s important to consult your doctor for proper interpretation.

Are there precautions to be taken before or after undergoing the test?

No specific precautions are required for this test. However, it's always best to follow the doctor's instructions and communicate any medications or supplements being taken.

What factors can affect the results of this test?

Modifiable Factors: Some medications and treatments such as chemotherapy can affect the levels.

Non-modifiable Factors: Age, gender, and genetic makeup can also influence the levels.

Which doctor should I consult if the test values are abnormal?

In case of abnormal results, it is recommended to consult a geneticist or an oncologist.

Are there any risks associated with Smart Cytogenetics 6?

The risks are minimal and typically related to the blood draw, such as minor pain or bruising at the site where the needle was inserted.

Can Smart Cytogenetics 6 detect more than one genetic disorder?

Yes, by analyzing six markers, Smart Cytogenetics 6 can detect a range of genetic disorders and abnormalities.

How is the blood sample collected for Smart Cytogenetics 6?

A blood sample is collected from a vein in your arm using a needle. This procedure is standard and carried out by a healthcare professional.

What is the difference between Karyotyping and FISH?

Karyotyping gives a broad view of the chromosomes, showing the number and structure, while FISH is more targeted, identifying specific DNA sequences for the presence of particular genetic mutations.

Can this test be used in prenatal diagnosis?

Yes, Smart Cytogenetics 6 can also be used in prenatal diagnosis for detecting chromosomal abnormalities in the fetus. However, the sample would typically be amniotic fluid or cells from the placenta.

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