ARHGAP31 Gene Adams-Oliver Syndrome Type 1 NGS Genetic DNA Test
Introduction
The ARHGAP31 Gene Adams-Oliver Syndrome Type 1 NGS Genetic DNA Test is a cutting-edge diagnostic tool designed to identify mutations in the ARHGAP31 gene, which is associated with Adams-Oliver syndrome. This genetic condition can lead to significant health challenges, including skin and skeletal abnormalities. Early detection through this test allows for timely interventions and management strategies, improving patient outcomes.
What the Test Measures
This test specifically measures the presence of mutations in the ARHGAP31 gene. By utilizing Next Generation Sequencing (NGS) technology, we can accurately detect these genetic variations that may lead to Adams-Oliver syndrome.
Who Should Consider This Test?
Individuals who may benefit from the ARHGAP31 Gene Adams-Oliver Syndrome Type 1 NGS Genetic DNA Test include:
- Patients exhibiting symptoms of Adams-Oliver syndrome, such as limb malformations and scalp defects.
- Individuals with a family history of genetic disorders related to the ARHGAP31 gene.
- Those seeking genetic counseling for family planning purposes.
Benefits of Taking the Test
- Provides definitive diagnosis of Adams-Oliver syndrome.
- Guides treatment and management options for affected individuals.
- Offers valuable information for family planning and genetic counseling.
- Helps in understanding the risk of transmission to future generations.
Understanding Your Results
Upon completion of the test, results will be provided to you in a clear and understandable format. It is crucial to discuss these results with a qualified healthcare provider or genetic counselor to understand their implications and the next steps in management.
Test Pricing
Price Type | Amount (NGN) |
---|---|
Discount Price | 400,000 NGN |
Regular Price | 560,000 NGN |
Book the Test
Ready to take the next step in understanding your genetic health? Book the ARHGAP31 Gene Adams-Oliver Syndrome Type 1 NGS Genetic DNA Test today! Contact us at +2348077798758 or visit our website for more information.
Additional Information
Turnaround Time: 3 to 4 Weeks
Sample Type: Blood or Extracted DNA or One drop Blood on FTA Card
Pre-Test Instructions: A clinical history review and a genetic counseling session to draw a pedigree chart of family members affected by the ARHGAP31 gene are recommended.