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FISH for CEP8 is a diagnostic test that uses a technique called Fluorescence In Situ Hybridization (FISH) to detect changes in chromosome 8. The “CEP” in CEP8 stands for “Chromosome Enumeration Probe,” which helps to identify the number of copies of chromosome 8 in the cells. The test is particularly useful in the diagnosis and monitoring of various medical conditions and diseases that are associated with abnormal changes in chromosome 8.

Chromosome 8 is known to harbor several genes that are crucial for cell growth and development. Anomalies in chromosome 8, such as having extra copies (Trisomy 8), can be associated with various disorders and cancers. Therefore, FISH for CEP8 is an important diagnostic tool that aids doctors in making informed decisions regarding treatment and management.

  • Test NameFISH for CEP8
  • Sample TypeBlood or Bone Marrow
  • Preparations RequiredNo specific preparation is required for this test. It’s important to follow any instructions your doctor might give.
  • Report Time5 days

What is the FISH for CEP8 test used for?

The test is used to detect abnormalities in chromosome 8, which can be linked to certain types of cancers and developmental disorders. It is crucial in diagnosis, prognosis, and in some cases, guiding the treatment decisions.

Is fasting required for the test?

No, fasting is not required for the FISH for CEP8 test.

Home Sample Collection Process

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Sample Collection by Phlebotomist
Sample Collection by Phlebotomist
Reporting of the sample at lab
Reporting of the sample at lab
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Download Reports
Frequently Asked Questions

A doctor may recommend this test if there is a suspicion of a disorder or cancer that is known to be associated with chromosome 8 anomalies. It may also be used to monitor the progression of certain diseases.

The test provides information on the number of copies of chromosome 8 in cells. It helps in detecting any abnormal changes that might be associated with diseases.

The sample is usually collected through a blood draw or bone marrow aspiration.

There are minimal risks associated with the blood draw, such as bruising or infection at the needle site. If a bone marrow sample is taken, there might be additional risks and discomfort.

The frequency of this test depends on the doctor’s recommendation, which is usually based on the underlying condition being investigated or monitored.

Normally, cells should have two copies of chromosome 8. Abnormal results might indicate an increased number of copies or other structural abnormalities in chromosome 8.

The levels can be affected by various factors including genetic mutations, cancers, and other underlying health conditions.

No special precautions are needed. However, it is important to inform your doctor if you are taking any medications or have any existing health conditions.

If you have abnormal results, it is advisable to consult a geneticist or a hematologist, depending on the context in which the test was ordered.

Abnormal results may indicate the presence of a genetic disorder or an increased risk of developing certain types of cancer. The information is crucial for diagnosis and deciding the further course of action.

There is no known interaction of medications with the test. However, it is always advisable to inform your doctor about any medications you are taking.

While FISH for CEP8 provides important information, it is usually not the sole basis for diagnosis. It might be used in conjunction with other tests and clinical evaluations.

Yes, this test can be done during pregnancy if there is a medical indication, such as suspicion of a genetic disorder. Consult your doctor for advice.

FISH for CEP8 is a significant diagnostic tool that helps in the detection of chromosome 8 abnormalities. By providing critical information on genetic changes, it plays a vital role in the diagnosis and monitoring of several diseases and disorders. Consulting a doctor for interpretation of results is essential to understand the implications and to receive appropriate guidance and care.

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