ZBTB16 Gene Leukemia Acute Promyelocytic PL2FRARA Type Genetic Test
Welcome to DNA Labs UAE, your trusted genetic lab in UAE. Today, we will be discussing the ZBTB16 Gene Leukemia Acute Promyelocytic PL2FRARA Type Genetic Test, its cost, symptoms, diagnosis, and other important details.
Test Name: ZBTB16 Gene Leukemia Acute Promyelocytic PL2FRARA Type Genetic Test
Components:
- Price: 4400.0 AED
- Sample Condition: Blood or Extracted DNA or One drop Blood on FTA Card
- Report Delivery: 3 to 4 Weeks
- Method: NGS Technology
- Test Type: Cancer
- Doctor: Oncologist
- Test Department: Genetics
Pre Test Information:
Before undergoing the ZBTB16 Gene Leukemia Acute Promyelocytic PL2FRARA Type Genetic Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session may be conducted to draw a pedigree chart of family members affected with ZBTB16 Gene Leukemia Acute Promyelocytic PL2FRARA Type NGS Genetic DNA Test gene ZBTB16.
Test Details:
The ZBTB16 gene, also known as PLZF (promyelocytic leukemia zinc finger), plays a crucial role in the development and function of various cell types, including immune cells and stem cells. Mutations or alterations in the ZBTB16 gene have been associated with different types of leukemia, including acute promyelocytic leukemia (APL).
APL is a subtype of acute myeloid leukemia (AML) characterized by the fusion of the promyelocytic leukemia (PML) gene with the retinoic acid receptor alpha (RARA) gene. This fusion gene, known as PML-RARA, disrupts normal cellular processes and leads to the development of leukemia.
Next-Generation Sequencing (NGS) genetic testing is a cutting-edge technique that allows for the simultaneous analysis of multiple genes. It helps identify mutations or alterations that may be associated with a particular disease or condition. In the case of APL, NGS genetic testing can detect the presence of the PML-RARA fusion gene, as well as other genetic abnormalities relevant for diagnosis, prognosis, or treatment decisions.
Therefore, the ZBTB16 gene test, specifically targeting the PL2F/RARA type, involves the analysis of the ZBTB16 gene and the detection of the PL2F/RARA fusion gene using NGS technology. This test provides valuable information for the diagnosis and management of APL patients.
If you are concerned about ZBTB16 Gene Leukemia Acute Promyelocytic PL2FRARA Type, we are here to help. Our experienced oncologists and genetic testing experts at DNA Labs UAE are dedicated to providing accurate and timely results to assist in your diagnosis and treatment decisions.
Contact us today to schedule your ZBTB16 Gene Leukemia Acute Promyelocytic PL2FRARA Type Genetic Test. Your health is our priority!
Test Name | ZBTB16 Gene Leukemia acute promyelocytic PL2FRARA type Genetic Test |
---|---|
Components | |
Price | 4400.0 AED |
Sample Condition | Blood or Extracted DNA or One drop Blood on FTA Card |
Report Delivery | 3 to 4 Weeks |
Method | NGS Technology |
Test type | Cancer |
Doctor | Oncologist |
Test Department: | Genetics |
Pre Test Information | Clinical History of Patient who is going for ZBTB16 Gene Leukemia, acute promyelocytic, PL2F/RARA type NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with ZBTB16 Gene Leukemia, acute promyelocytic, PL2F/RARA type NGS Genetic DNA Test gene ZBTB16 |
Test Details |
The ZBTB16 gene, also known as PLZF (promyelocytic leukemia zinc finger), is involved in the development and function of various cell types, including immune cells and stem cells. Mutations or alterations in the ZBTB16 gene have been associated with different types of leukemia, including acute promyelocytic leukemia (APL). APL is a subtype of acute myeloid leukemia (AML) characterized by the fusion of the promyelocytic leukemia (PML) gene with the retinoic acid receptor alpha (RARA) gene. This fusion gene, known as PML-RARA, disrupts normal cellular processes and leads to the development of leukemia. NGS (Next-Generation Sequencing) genetic testing is a technique used to analyze multiple genes simultaneously and identify mutations or alterations that may be associated with a particular disease or condition. In the context of APL, NGS genetic testing can be used to detect the presence of the PML-RARA fusion gene, as well as other genetic abnormalities that may be relevant for diagnosis, prognosis, or treatment decisions. Therefore, a ZBTB16 gene test, specifically targeting the PL2F/RARA type, would involve the analysis of the ZBTB16 gene and the detection of the PL2F/RARA fusion gene using NGS technology. This test can provide valuable information for the diagnosis and management of APL patients. |