Smart Cytogenetics 5: Karyotyping and FISH for Five Markers

Individuals who are suspected of having genetic disorders, or patients with certain types of cancers, especially those involving multiple genetic alterations, may be advised to take this test.

Smart Cytogenetics 5 offers detailed information on the structure and number of chromosomes, and it can detect specific genetic abnormalities by analyzing five different markers.

The frequency of this test varies depending on the patient’s condition and the doctor's recommendations. It might be performed periodically for monitoring in cases of chronic disorders or cancers.

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

No specific precautions are required for this test. However, patients should always follow the doctor's instructions and communicate any medications or supplements they are taking.

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

Consultation with a geneticist or oncologist is recommended in case of abnormal results.

The risks are minimal and are generally associated with the blood draw, such as minor pain or bruising at the site of the needle.

Yes, analyzing five markers enables Smart Cytogenetics 5 to detect multiple genetic disorders and abnormalities.

The blood sample is collected from a vein in the arm using a needle. This is a standard procedure performed by a medical professional.

Yes, this test can be performed on patients of all ages, including children, especially if there is a suspicion of a genetic disorder.

Karyotyping provides an overall view of the chromosomes, while FISH is more targeted and can detect specific genetic mutations or changes in DNA.