ERCC6L2 Gene Bone Marrow Failure Syndrome Type 2 Genetic Test sale cost 4400 AED
ASXL1 Gene Bohring-Opitz Syndrome Genetic Test sale cost 4400 AED ASXL1 Gene Bohring-Opitz Syndrome Genetic Test Cost 5,600 د.إ Original price was: 5,600 د.إ.4,400 د.إCurrent price is: 4,400 د.إ.
BDNF Gene Central Hypoventilation Syndrome Congenital Genetic Test sale cost 4400 AED BDNF Gene Central Hypoventilation Syndrome Congenital Genetic Test Cost 5,600 د.إ Original price was: 5,600 د.إ.4,400 د.إCurrent price is: 4,400 د.إ.
Sale!

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, which are associated with Bone Marrow Failure Syndrome Type 2. This condition is a rare genetic disorder that can lead to serious complications including anemia, increased risk of infections, and a higher likelihood of developing leukemia. Early and accurate diagnosis through this genetic test enables healthcare providers to tailor treatment plans more effectively, improving patient outcomes.

The test is priced at 4400 AED and involves collecting a DNA sample, typically through a blood draw, which is then analyzed in the laboratory for specific genetic alterations in the ERCC6L2 gene. The results of this test can provide crucial information for the management of the condition, including guidance on monitoring strategies and treatment options to address the symptoms and prevent complications. DNA Labs UAE employs state-of-the-art technology and follows stringent protocols to ensure the accuracy and reliability of the test results, making it a trusted choice for patients and healthcare providers seeking comprehensive insights into Bone Marrow Failure Syndrome Type 2.

Home  Sample collection service available

  • 100% accuaret Test Results
  • Ranked as Most trusted Genetic DNA Lab
  • This test is not intended for medical diagnosis or treatment
Guaranteed Safe Checkout

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.

SKU: TEST-4011 Category:

Related products