NRAS Gene Noonan Syndrome Type 6 NGS Genetic DNA Test
Comprehensive Genetic Testing for Noonan Syndrome Type 6
The NRAS Gene Noonan Syndrome Type 6 NGS Genetic DNA Test represents a cutting-edge diagnostic approach for identifying mutations in the NRAS gene that cause Noonan Syndrome Type 6. This rare genetic disorder affects multiple body systems and requires precise genetic confirmation for accurate diagnosis and management. Our advanced Next-Generation Sequencing technology provides comprehensive analysis of the NRAS gene, enabling healthcare providers to make informed decisions about patient care and treatment strategies.
What Does This Test Measure?
This specialized genetic test specifically targets the NRAS gene, which plays a critical role in the RAS/MAPK signaling pathway. The test detects:
- Pathogenic variants in the NRAS gene associated with Noonan Syndrome Type 6
- Single nucleotide variants (SNVs) and small insertions/deletions
- Genetic mutations affecting protein function and cellular signaling
- Variants that disrupt normal developmental processes
Who Should Consider This Test?
This genetic test is recommended for individuals presenting with symptoms suggestive of Noonan Syndrome Type 6, including:
- Characteristic facial features (hypertelorism, ptosis, low-set ears)
- Congenital heart defects, particularly pulmonary valve stenosis
- Growth delays and short stature
- Developmental delays and learning difficulties
- Feeding difficulties in infancy
- Cryptorchidism in males
- Bleeding tendencies and coagulation abnormalities
- Family history of Noonan Syndrome or related conditions
Clinical Benefits of NRAS Gene Testing
Undergoing the NRAS Gene Noonan Syndrome Type 6 NGS Genetic DNA Test provides numerous clinical advantages:
- Accurate Diagnosis: Confirms or rules out Noonan Syndrome Type 6 with high precision
- Personalized Treatment: Enables targeted management strategies based on genetic findings
- Family Planning: Provides crucial information for genetic counseling and reproductive decisions
- Early Intervention: Facilitates timely implementation of appropriate therapies and monitoring
- Comprehensive Care: Guides multidisciplinary approach involving cardiology, endocrinology, and developmental specialists
Understanding Your Test Results
Your genetic test results will be carefully interpreted by our team of certified genetic counselors and medical geneticists. Results typically fall into one of these categories:
- Positive Result: Identifies a pathogenic variant in the NRAS gene, confirming Noonan Syndrome Type 6 diagnosis
- Negative Result: No disease-causing variants detected, though clinical evaluation remains important
- Variant of Uncertain Significance (VUS): Identifies a genetic change whose clinical significance requires further investigation
- Carrier Status: May identify individuals carrying NRAS gene variants
All positive results include detailed interpretation and recommendations for follow-up care and family testing.
Test Pricing Information
| Test Description | Price (USD) |
|---|---|
| NRAS Gene Noonan Syndrome Type 6 NGS Genetic DNA Test – Discount Price | $500 |
| NRAS Gene Noonan Syndrome Type 6 NGS Genetic DNA Test – Regular Price | $700 |
Nationwide Testing Availability
We proudly offer the NRAS Gene Noonan Syndrome Type 6 NGS Genetic DNA Test across the United States, with convenient testing locations in all major metropolitan areas including New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, and San Jose. Our network of certified collection centers ensures accessible genetic testing services for patients nationwide.
Book Your Genetic Test Today
Take the first step toward accurate diagnosis and personalized care. Our experienced genetic counselors are available to discuss your testing needs and answer any questions about the NRAS Gene Noonan Syndrome Type 6 NGS Genetic DNA Test.
Call or WhatsApp us today at +1(267) 388-9828 to schedule your appointment or learn more about our comprehensive genetic testing services.
With a turnaround time of 3-4 weeks and multiple sample collection options including blood, extracted DNA, or blood spots on FTA cards, we make genetic testing convenient and accessible. Pre-test genetic counseling is recommended to review family history and ensure appropriate test selection.
