Smart Cytogenetics 6: Karyotyping and FISH for Six Markers

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.

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.

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.

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.

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.

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

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

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.

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

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.

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.

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.