MYCN Gene Feingold Syndrome NGS Genetic DNA Test
Comprehensive Genetic Analysis for Developmental Disorders
The MYCN Gene Feingold Syndrome NGS Genetic DNA Test represents a cutting-edge diagnostic tool in pediatric genetics, utilizing next-generation sequencing technology to identify mutations in the MYCN gene associated with Feingold syndrome. This rare autosomal dominant disorder affects multiple body systems and requires precise genetic confirmation for accurate diagnosis and management.
What Does This Test Detect?
This advanced genetic test specifically targets the MYCN gene, which plays a critical role in embryonic development and cellular differentiation. The test identifies:
- Point mutations in the MYCN gene coding regions
- Small insertions and deletions affecting gene function
- Pathogenic variants associated with Feingold syndrome
- Genetic changes impacting protein structure and function
Who Should Consider This Test?
Clinical Indications and Symptoms
This genetic test is recommended for individuals presenting with the following clinical features:
- Developmental Delays: Cognitive and motor development concerns
- Microcephaly: Abnormally small head circumference
- Limb Abnormalities: Shortening of fingers and toes (brachymesophalangy)
- Gastrointestinal Issues: Esophageal and duodenal atresia
- Facial Dysmorphism: Characteristic facial features including short palpebral fissures
- Family History: Known or suspected Feingold syndrome in relatives
Benefits of Genetic Testing
Undergoing the MYCN Gene Feingold Syndrome test provides numerous advantages:
- Definitive Diagnosis: Confirms or rules out Feingold syndrome with high accuracy
- Personalized Management: Enables targeted treatment and monitoring strategies
- Family Planning: Provides crucial information for genetic counseling and reproductive decisions
- Early Intervention: Facilitates timely therapeutic interventions for better outcomes
- Prognostic Information: Helps predict disease progression and potential complications
Understanding Your Test Results
Interpreting Genetic Findings
Your test results will be thoroughly explained by our genetic counselors:
- Positive Result: Identifies a pathogenic MYCN mutation confirming Feingold syndrome diagnosis
- Negative Result: No disease-causing mutation detected, though clinical correlation remains essential
- Variant of Uncertain Significance: Identifies genetic changes requiring further investigation
- Carrier Status: Important information for family members and future pregnancies
Test Details and Pricing
| Test Parameter | Details |
|---|---|
| Test Name | MYCN Gene Feingold Syndrome NGS Genetic DNA Test |
| Discount Price | $500 USD |
| Regular Price | $700 USD |
| Turnaround Time | 3 to 4 Weeks |
| Sample Type | Blood, Extracted DNA, or One Drop Blood on FTA Card |
| Testing Method | Next-Generation Sequencing (NGS) |
| Specialty | Pediatric Genetics |
Pre-Test Requirements
Before scheduling your test, please ensure:
- Complete clinical history of the patient
- Genetic counseling session to create a detailed family pedigree
- Discussion of testing implications and potential outcomes
- Informed consent for genetic testing
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 consistent, high-quality care regardless of location.
Take the Next Step Toward Genetic Clarity
Don’t let uncertainty about developmental concerns affect your family’s future. Our comprehensive MYCN Gene Feingold Syndrome testing provides the answers you need for informed medical decisions and personalized care planning.
Call or WhatsApp us today at +1(267) 388-9828 to schedule your genetic test consultation and take control of your genetic health journey.
Our dedicated team of genetic specialists is ready to guide you through the testing process, answer your questions, and provide the support your family deserves. Book your appointment now and begin your path to genetic clarity and peace of mind.
