ARHGAP31 Gene Adams-Oliver Syndrome Type 1 NGS Genetic DNA Test
Comprehensive Genetic Testing for Rare Congenital Disorders
The ARHGAP31 Gene Adams-Oliver Syndrome Type 1 NGS Genetic DNA Test represents a breakthrough in genetic diagnostics for rare congenital conditions. This advanced testing methodology provides definitive answers for individuals and families affected by Adams-Oliver Syndrome Type 1, a complex disorder affecting multiple body systems including skin, bone, and vascular development.
What Does This Test Measure and Detect?
Our specialized NGS genetic test specifically targets the ARHGAP31 gene, which plays a crucial role in cellular signaling and development. The test identifies:
- Pathogenic mutations in the ARHGAP31 gene
- Single nucleotide variants (SNVs) associated with Adams-Oliver Syndrome
- Small insertions and deletions affecting gene function
- Copy number variations that may impact disease manifestation
- Genetic markers for inheritance pattern determination
Who Should Consider This Genetic Test?
This comprehensive genetic analysis is recommended for individuals presenting with:
- Congenital scalp defects (cutis aplasia)
- Limb abnormalities including shortened fingers or toes
- Vascular malformations or abnormalities
- Family history of Adams-Oliver Syndrome
- Unexplained developmental delays with characteristic physical features
- Planning pregnancy with known family history of the condition
Clinical Benefits of Genetic Testing
Undergoing the ARHGAP31 genetic test provides numerous advantages:
- Accurate Diagnosis: Confirm or rule out Adams-Oliver Syndrome Type 1 with precision
- Family Planning: Make informed reproductive decisions based on genetic risk
- Personalized Care: Develop targeted treatment and management strategies
- Early Intervention: Implement appropriate medical monitoring and interventions
- Genetic Counseling: Receive comprehensive guidance for family members
Understanding Your Test Results
Our genetic specialists provide detailed interpretation of your results:
- Positive Result: Indicates the presence of pathogenic ARHGAP31 mutations, confirming Adams-Oliver Syndrome Type 1 diagnosis
- Negative Result: Suggests absence of known disease-causing mutations in the ARHGAP31 gene
- Variant of Uncertain Significance: Identifies genetic changes with unknown clinical impact requiring further evaluation
- Carrier Status: Determines if you carry the genetic mutation without showing symptoms
Test Pricing and Details
| Test Component | Price (USD) |
|---|---|
| Discount Price | $500 |
| Regular Price | $700 |
| Turnaround Time | 3-4 Weeks |
| Sample Type | Blood, Extracted DNA, or One Drop Blood on FTA Card |
Nationwide Testing Availability
We proudly serve patients across the United States with convenient testing locations in all major cities including New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, San Jose, and many more. Our network of certified genetic counselors and medical professionals ensures you receive comprehensive care regardless of your location.
Take the Next Step Toward Genetic Clarity
Don’t let uncertainty about genetic conditions affect your health decisions. Our ARHGAP31 Gene Adams-Oliver Syndrome Type 1 NGS Genetic DNA Test provides the definitive answers you need for proper diagnosis and management. With our discounted price of $500 and comprehensive genetic counseling services, you can make informed decisions about your health and family planning.
Call us today at +1(267) 388-9828 to schedule your genetic test or speak with our genetic counseling team. Take control of your genetic health with confidence and precision.
