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ASXL1 Gene Bohring-Opitz Syndrome Genetic Test Cost

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

-21%

The ASXL1 gene Bohring-Opitz Syndrome genetic test is a specialized diagnostic tool designed to identify mutations in the ASXL1 gene, which are linked to Bohring-Opitz Syndrome (BOS). This rare genetic disorder is characterized by distinctive facial features, growth delays, intellectual disability, and various physical abnormalities. Early detection through this test can aid in the management and treatment of the condition.

Conducted at DNA Labs UAE, a leading facility in genetic diagnostics, the test employs advanced genomic technologies to analyze the ASXL1 gene for any alterations that might indicate the presence of BOS. The process involves collecting a DNA sample, usually through a blood draw or cheek swab, which is then meticulously examined for specific genetic mutations associated with the syndrome.

The cost of the ASXL1 gene Bohring-Opitz Syndrome genetic test at DNA Labs UAE is 4400 AED. This price reflects the comprehensive nature of the test, encompassing the sophisticated analysis and the expertise required to interpret the results accurately. Given the complexity of genetic disorders like BOS, having access to such precise diagnostic tools is invaluable for affected families, offering insights into potential treatment paths and helping to manage the condition more effectively.

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
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ASXL1 Gene Bohring-Opitz syndrome Genetic Test

At DNA Labs UAE, we offer the ASXL1 Gene Bohring-Opitz syndrome Genetic Test at a cost of AED 4400.0. This test is designed to diagnose Bohring-Opitz syndrome, a rare genetic disorder characterized by severe developmental delay, intellectual disability, distinctive facial features, and other physical abnormalities.

Test Components

The ASXL1 Gene Bohring-Opitz syndrome Genetic Test includes the following components:

  • NGS Technology
  • Dysmorphology Test Type
  • Pediatrics Doctor
  • Genetics Test Department

Sample Condition

We accept blood or extracted DNA samples for this test. Alternatively, one drop of blood on an FTA Card can also be used.

Report Delivery

The test results will be delivered within 3 to 4 weeks.

Method

We utilize NGS Technology for this genetic test.

Pre Test Information

Prior to undergoing the ASXL1 Gene Bohring-Opitz syndrome 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 by ASXL1 Gene Bohring-Opitz syndrome.

Test Details

The ASXL1 gene is associated with Bohring-Opitz syndrome. Our NGS genetic testing analyzes the DNA sequence of genes, including ASXL1, to identify any mutations or abnormalities that may be causing the syndrome. This diagnostic tool is invaluable in diagnosing Bohring-Opitz syndrome and guiding appropriate medical management and genetic counseling for affected individuals and their families.

Test Name ASXL1 Gene Bohring-Opitz syndrome 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 ASXL1 Gene Bohring-Opitz syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with ASXL1 Gene Bohring-Opitz syndrome NGS Genetic DNA Test gene ASXL1
Test Details

The ASXL1 gene is associated with Bohring-Opitz syndrome, a rare genetic disorder characterized by severe developmental delay, intellectual disability, distinctive facial features, and other physical abnormalities. NGS (Next-Generation Sequencing) genetic testing is a diagnostic tool used to analyze the DNA sequence of genes, including the ASXL1 gene, to identify any mutations or abnormalities that may be causing the syndrome. This type of testing can provide valuable information for diagnosing Bohring-Opitz syndrome and guiding appropriate medical management and genetic counseling for affected individuals and their families.

SKU: TEST-4010 Category:

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