ERCC6L2 Gene Bone Marrow Failure Syndrome Type 2 Genetic Test
At DNA Labs UAE, we offer the ERCC6L2 Gene Bone Marrow Failure Syndrome Type 2 Genetic Test. This test is designed to detect mutations or variations in the ERCC6L2 gene that are associated with bone marrow failure syndrome type 2. The test utilizes Next-Generation Sequencing (NGS) technology to analyze the DNA sequence of the ERCC6L2 gene and identify any genetic changes that may be present.
Test Components and Price
- Test Name: ERCC6L2 Gene Bone Marrow Failure Syndrome Type 2 Genetic Test
- Components: NGS Technology
- Price: 4400.0 AED
Sample Condition and Report Delivery
- Sample Condition: Blood or Extracted DNA or One drop Blood on FTA Card
- Report Delivery: 3 to 4 Weeks
Test Type and Doctor
- Test Type: Dysmorphology
- Doctor: Pediatrics
Test Department and Pre Test Information
- Test Department: Genetics
- Pre Test Information: Clinical History of Patient who is going for ERCC6L2 Gene Bone Marrow Failure Syndrome Type 2 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with ERCC6L2 Gene Bone Marrow Failure Syndrome Type 2 NGS Genetic DNA Test gene ERCC6L2
Test Details
The ERCC6L2 gene bone marrow failure syndrome type 2 NGS genetic test is a type of genetic test that is used to detect mutations or variations in the ERCC6L2 gene that are associated with bone marrow failure syndrome type 2. This genetic test uses Next-Generation Sequencing (NGS) technology to analyze the DNA sequence of the ERCC6L2 gene and identify any genetic changes that may be present.
Bone marrow failure syndrome type 2 is a rare genetic disorder characterized by a progressive failure of the bone marrow to produce an adequate number of blood cells. This can lead to a variety of symptoms, including anemia, fatigue, increased susceptibility to infections, and bleeding problems.
The ERCC6L2 gene is involved in the repair of damaged DNA. Mutations or variations in this gene can disrupt its normal function, leading to the development of bone marrow failure syndrome type 2.
The NGS genetic test for ERCC6L2 gene bone marrow failure syndrome type 2 can help in the diagnosis of this condition, as well as in providing information about the prognosis and potential treatment options. It can also be used for genetic counseling and to determine the risk of passing on the condition to future generations.
It is important to note that this genetic test should be ordered and interpreted by a qualified healthcare professional, such as a geneticist or genetic counselor, who can provide appropriate counseling and guidance based on the test results.
Test Name | ERCC6L2 Gene Bone marrow failure syndrome type 2 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 | Dysmorphology |
Doctor | Pediatrics |
Test Department: | Genetics |
Pre Test Information | Clinical History of Patient who is going for ERCC6L2 Gene Bone marrow failure syndrome type 2 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with ERCC6L2 Gene Bone marrow failure syndrome type 2 NGS Genetic DNA Test gene ERCC6L2 |
Test Details |
ERCC6L2 gene bone marrow failure syndrome type 2 NGS genetic test is a type of genetic test that is used to detect mutations or variations in the ERCC6L2 gene that are associated with bone marrow failure syndrome type 2. This genetic test uses Next-Generation Sequencing (NGS) technology to analyze the DNA sequence of the ERCC6L2 gene and identify any genetic changes that may be present. Bone marrow failure syndrome type 2 is a rare genetic disorder characterized by a progressive failure of the bone marrow to produce an adequate number of blood cells. This can lead to a variety of symptoms, including anemia, fatigue, increased susceptibility to infections, and bleeding problems. The ERCC6L2 gene is involved in the repair of damaged DNA. Mutations or variations in this gene can disrupt its normal function, leading to the development of bone marrow failure syndrome type 2. The NGS genetic test for ERCC6L2 gene bone marrow failure syndrome type 2 can help in the diagnosis of this condition, as well as in providing information about the prognosis and potential treatment options. It can also be used for genetic counseling and to determine the risk of passing on the condition to future generations. It is important to note that this genetic test should be ordered and interpreted by a qualified healthcare professional, such as a geneticist or genetic counselor, who can provide appropriate counseling and guidance based on the test results. |