MIR17HG Gene Feingold Syndrome Type 2 NGS Genetic DNA Test
Comprehensive Genetic Analysis for Developmental Disorders
The MIR17HG Gene Feingold Syndrome Type 2 NGS Genetic DNA Test represents a cutting-edge diagnostic tool that utilizes next-generation sequencing technology to identify mutations in the MIR17HG gene. This specialized genetic test plays a crucial role in diagnosing Feingold Syndrome Type 2, a rare genetic disorder characterized by multiple physical abnormalities and developmental challenges. By providing precise genetic information, this test enables healthcare providers to establish accurate diagnoses and develop targeted treatment strategies.
What Does This Test Measure and Detect?
This advanced genetic screening specifically targets the MIR17HG gene, which encodes a microRNA cluster essential for normal embryonic development and cellular regulation. The test detects:
- Pathogenic variants and mutations in the MIR17HG gene
- Single nucleotide polymorphisms (SNPs) associated with Feingold Syndrome Type 2
- Copy number variations affecting gene function
- Structural abnormalities within the gene sequence
- Inheritance patterns for family planning purposes
Who Should Consider This Genetic Test?
This specialized genetic testing is recommended for individuals presenting with symptoms suggestive of Feingold Syndrome Type 2, including:
- Children with unexplained growth retardation and developmental delays
- Individuals with characteristic digital anomalies such as shortened fingers or toes
- Patients with microcephaly (small head circumference)
- Those exhibiting distinctive facial features including a small jaw and prominent nasal bridge
- Individuals with gastrointestinal abnormalities or feeding difficulties
- Patients with family history of similar developmental disorders
- Couples planning pregnancy with known family history of genetic disorders
Key Benefits of MIR17HG Genetic Testing
Undergoing this comprehensive genetic analysis provides numerous advantages for patients and healthcare providers:
- Accurate Diagnosis: Confirms or rules out Feingold Syndrome Type 2 with high precision
- Personalized Treatment Planning: Enables targeted interventions based on specific genetic findings
- Family Planning Guidance: Provides crucial information for reproductive decisions and genetic counseling
- Early Intervention: Facilitates timely medical management and supportive care
- Comprehensive Analysis: Utilizes advanced NGS technology for thorough genetic assessment
- Peace of Mind: Reduces diagnostic uncertainty and provides clear answers
Understanding Your Test Results
Your genetic test results will be carefully interpreted by our team of certified genetic specialists. Positive results indicating MIR17HG gene mutations confirm the diagnosis of Feingold Syndrome Type 2 and provide valuable information about the specific genetic variant involved. Negative results help rule out this specific genetic condition, allowing healthcare providers to explore alternative diagnoses. All results include detailed explanations and recommendations for next steps, including potential referrals to specialists in osteology, dermatology, and immunology as needed.
Test Pricing and Availability
| Test Name | Discount Price | Regular Price |
|---|---|---|
| MIR17HG Gene Feingold Syndrome Type 2 NGS Genetic DNA Test | $500 USD | $700 USD |
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 state-of-the-art laboratories ensure consistent, high-quality testing regardless of your location.
Take Control of Your Genetic Health Today
Don’t let uncertainty about genetic conditions affect your quality of life. Our MIR17HG Gene Feingold Syndrome Type 2 NGS Genetic DNA Test provides the clarity and answers you need for informed healthcare decisions. With results available in just 3-4 weeks and multiple sample collection options including blood, extracted DNA, or simple blood spot cards, getting tested has never been more convenient.
Ready to schedule your genetic test? Contact our genetic counseling team today at +1(267) 388-9828 or book your appointment online. Our specialists are available to answer your questions and guide you through the testing process with compassion and expertise.
