RASA1 Gene Parkes Weber Syndrome NGS Genetic DNA Test
Comprehensive Genetic Testing for Vascular Disorders
The RASA1 Gene Parkes Weber Syndrome NGS Genetic DNA Test represents a cutting-edge diagnostic approach for identifying genetic mutations associated with Parkes Weber syndrome, a rare congenital disorder characterized by complex vascular malformations. This sophisticated genetic analysis utilizes next-generation sequencing technology to provide comprehensive evaluation of the RASA1 gene, which plays a critical role in regulating blood vessel development and cellular signaling pathways.
What Does This Test Measure and Detect?
This advanced genetic test specifically targets and analyzes the RASA1 gene (RAS p21 protein activator 1) to identify pathogenic variants responsible for Parkes Weber syndrome. The test detects:
- Point mutations, deletions, and insertions in the RASA1 gene
- Genetic variations affecting the RAS-MAPK signaling pathway
- Mutations that disrupt normal blood vessel formation and development
- Inherited and de novo genetic changes associated with vascular malformations
Who Should Consider This Genetic Test?
This test is recommended for individuals presenting with clinical features suggestive of Parkes Weber syndrome or related vascular disorders:
- Patients with limb hypertrophy or overgrowth affecting arms or legs
- Individuals with cutaneous capillary malformations (port-wine stains)
- Those diagnosed with arteriovenous fistulas or malformations
- Patients with family history of vascular anomalies or genetic disorders
- Individuals experiencing complications from vascular abnormalities
- Children presenting with congenital limb enlargement and vascular stains
Key Benefits of RASA1 Genetic Testing
Undergoing this comprehensive genetic analysis provides numerous advantages for patients and healthcare providers:
- Accurate Diagnosis: Confirms or rules out Parkes Weber syndrome with high precision
- Personalized Treatment Planning: Enables targeted management strategies based on genetic findings
- Family Risk Assessment: Identifies inheritance patterns and assesses risk for family members
- Early Intervention: Facilitates timely management of potential complications
- Reproductive Counseling: Provides valuable information for family planning decisions
- Comprehensive Care Coordination: Supports multidisciplinary approach to vascular disorder management
Understanding Your Test Results
Your genetic test results will be carefully interpreted by our expert genetic counselors and medical specialists:
- Positive Result: Indicates the presence of a pathogenic RASA1 gene mutation, confirming Parkes Weber syndrome diagnosis
- Negative Result: Suggests no detectable RASA1 mutation, though clinical evaluation remains important
- Variant of Uncertain Significance: Identifies genetic changes requiring further clinical correlation
- Carrier Status: Determines if you carry a single copy of a mutated gene
All results include detailed explanations and recommendations for next steps in your healthcare journey.
Test Pricing Information
| Test Description | Price (USD) |
|---|---|
| RASA1 Gene Parkes Weber Syndrome NGS Genetic DNA Test – Discount Price | $500 |
| RASA1 Gene Parkes Weber Syndrome NGS Genetic DNA Test – Regular Price | $700 |
Nationwide Testing Availability
We proudly offer comprehensive genetic testing services across the United States with convenient locations in all major metropolitan areas including New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, San Jose, and many other cities. Our network of certified testing facilities ensures accessible, high-quality genetic analysis for patients nationwide.
Take the Next Step in Your Health Journey
Don’t let uncertainty about vascular symptoms delay your path to accurate diagnosis and effective treatment. Our expert genetic counseling team is ready to guide you through the testing process and help you understand your results. Schedule your RASA1 Gene Parkes Weber Syndrome NGS Genetic DNA Test today and gain the clarity needed for informed healthcare decisions.
Call us now at +1(267) 388-9828 to book your appointment or speak with our genetic specialists about this important diagnostic test.
