Smart Cytogenetics 1 - Karyotyping - FISH for One Marker Test, Price | Sprint Diagnostics Hyderabad

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

₹ 8000

Smart Cytogenetics 1 is a diagnostic test that involves two different techniques, Karyotyping and Fluorescence In Situ Hybridization (FISH) for one marker. These techniques help to analyze the chromosomes in a sample of blood cells. This test is particularly important in the diagnosis and monitoring of various genetic disorders and certain types of cancers. Karyotyping involves staining the chromosomes and examining them under a microscope. It helps in evaluating the number and structure of chromosomes. On the other hand, FISH uses fluorescent probes to detect specific DNA sequences on the chromosomes. This helps in identifying genetic abnormalities with greater precision.

Knowing the genetic makeup of cells, especially in cases of suspected genetic disorders or cancer, can be crucial in determining the most effective treatment approach. Smart Cytogenetics 1 is generally recommended by doctors to diagnose genetic diseases, evaluate the status of cancer, and sometimes to decide on the course of treatment.

Test Name Smart Cytogenetics 1: Karyotyping + FISH for One Marker
Sample Type Blood/ bone marrow
Preparations Required No special preparation is needed for this test.
Report Time 12 Days for Karyotype & 5 Days for FISH
Price in Hyderabad ₹ 8000

What is the importance of getting the Smart Cytogenetics 1 test done?

This test is essential for detecting and evaluating genetic abnormalities or changes in chromosomes. It can be used to diagnose genetic disorders, certain cancers, and can sometimes play a critical role in tailoring an individual's treatment plan.

Is fasting required for this test?

No, fasting is not required for the Smart Cytogenetics 1 test.

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Is there any specific preparation needed before taking this test?

There is no specific preparation needed for this test. It's always good to inform the doctor about any medications you are currently taking.

When is this test recommended?

This test is generally recommended when there is suspicion of a genetic disorder or to evaluate the genetic aspects of cancers. It may also be used to monitor the effectiveness of a treatment or check for recurrence of cancer.

What information does this test provide?

Smart Cytogenetics 1 provides information about the number and structure of chromosomes in the blood cells. It helps in identifying any genetic abnormalities which could be indicative of genetic disorders or cancers.

How often should this test be done?

The frequency of this test depends on the clinical condition of the patient and the doctor’s recommendations. In some cases, it might be a one-time test, while in others, especially in cancer patients, it might be done periodically to monitor the disease.

What are the normal values for this test?

Normal values indicate a normal number and structure of chromosomes. However, what is considered normal can vary. It is best to discuss the results with your doctor for a comprehensive understanding.

What precautions should be taken before and after the test?

There are no special precautions needed before or after the test. However, patients should inform their doctor of any medications they are taking.

What factors can affect the levels?

Modifiable Factors: Certain medications and chemotherapy can affect the test results.
Non-modifiable Factors: Age, gender, and genetic predisposition can also impact the results.

Which doctor should be consulted in case of abnormal values?

In case of abnormal values, it is advisable to consult a geneticist or an oncologist, depending on the context of the test.

What are the risks associated with this test?

As the test requires a blood sample, there are minimal risks associated with blood drawing, such as slight pain or bruising at the site of needle insertion.

Can this test detect cancer?

Yes, this test can help detect chromosomal abnormalities often associated with certain types of cancers.

How is the blood sample collected?

The blood sample is usually collected from a vein in the arm using a needle. It is a standard procedure and is done by a medical professional.

Can this test be used for prenatal screening?

Yes, but typically, a different sample such as amniotic fluid or placental tissue is used for prenatal screening.

Is this test conclusive for diagnoses?

While the test provides vital information about chromosomal structures and abnormalities, it is often considered along with other diagnostic information. Your doctor will consider these results as part of a broader diagnostic process.

Smart Cytogenetics 1 is a significant advancement in medical diagnostics. It not only helps in detecting genetic abnormalities but also plays an essential role in the management and treatment of various disorders and cancers. It is always advisable to discuss the necessity, process, and results of this test with your doctor to have a better understanding and to make informed decisions regarding your health.

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