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ERCC6L2 Gene Bone Marrow Failure Syndrome Type 2 Genetic Test Cost

Original price was: 5,600 د.إ.Current price is: 4,400 د.إ.

-21%

The ERCC6L2 Gene Bone Marrow Failure Syndrome Type 2 Genetic Test is a specialized diagnostic tool available at DNA Labs UAE, designed to identify mutations in the ERCC6L2 gene. These mutations are linked to a rare genetic disorder known as Bone Marrow Failure Syndrome Type 2. This condition can lead to a range of hematological issues, including an increased risk of developing certain types of cancer. The test plays a crucial role in the early detection and management of the syndrome, allowing healthcare providers to tailor treatments and interventions more effectively.

Conducted at DNA Labs UAE, a facility known for its state-of-the-art genetic testing services, the test involves collecting a DNA sample from the patient, usually through a blood draw. The sample is then analyzed to detect any abnormalities or mutations in the ERCC6L2 gene that could indicate the presence of Bone Marrow Failure Syndrome Type 2.

The cost of the ERCC6L2 Gene Bone Marrow Failure Syndrome Type 2 Genetic Test at DNA Labs UAE is set at 4400 AED. This price reflects the sophisticated technology and expert analysis required to accurately identify mutations in the ERCC6L2 gene. For patients at risk of this syndrome or exhibiting symptoms related to bone marrow failure, this test provides a critical pathway to understanding their condition and accessing appropriate care.

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ERCC6L2 Gene Bone Marrow Failure Syndrome Type 2 Genetic Test

Test Name: ERCC6L2 Gene Bone Marrow Failure Syndrome Type 2 Genetic Test

Components: ERCC6L2 gene analysis

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: Hematology

Doctor: Hematologist

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 genetic test that analyzes the ERCC6L2 gene for mutations or variations that are associated with bone marrow failure syndrome type 2. This syndrome is a rare genetic disorder characterized by a decrease in the production of blood cells in the bone marrow, leading to low blood cell counts and various symptoms such as fatigue, infections, and bleeding.

NGS (Next-Generation Sequencing) is a high-throughput DNA sequencing technology that allows for the simultaneous analysis of multiple genes or even the entire genome. In the case of the ERCC6L2 gene bone marrow failure syndrome type 2 NGS genetic test, it involves sequencing the ERCC6L2 gene to identify any mutations or variations that may be causing or contributing to the syndrome.

The test can be used to confirm a diagnosis in individuals suspected of having bone marrow failure syndrome type 2 based on their symptoms and medical history. It can also be used for carrier testing in family members of affected individuals or for prenatal testing in couples with a family history of the syndrome.

The results of the test can help guide treatment decisions and management strategies for individuals with bone marrow failure syndrome type 2. It can also provide valuable information for genetic counseling and family planning purposes.

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 Hematology
Doctor Hematologist
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 genetic test that analyzes the ERCC6L2 gene for mutations or variations that are associated with bone marrow failure syndrome type 2. This syndrome is a rare genetic disorder characterized by a decrease in the production of blood cells in the bone marrow, leading to low blood cell counts and various symptoms such as fatigue, infections, and bleeding.

NGS (Next-Generation Sequencing) is a high-throughput DNA sequencing technology that allows for the simultaneous analysis of multiple genes or even the entire genome. In the case of the ERCC6L2 gene bone marrow failure syndrome type 2 NGS genetic test, it involves sequencing the ERCC6L2 gene to identify any mutations or variations that may be causing or contributing to the syndrome.

The test can be used to confirm a diagnosis in individuals suspected of having bone marrow failure syndrome type 2 based on their symptoms and medical history. It can also be used for carrier testing in family members of affected individuals or for prenatal testing in couples with a family history of the syndrome.

The results of the test can help guide treatment decisions and management strategies for individuals with bone marrow failure syndrome type 2. It can also provide valuable information for genetic counseling and family planning purposes.

SKU: TEST-3875 Category:

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