GDF3 Gene Klippel-Feil Syndrome Type 3 Autosomal Dominant NGS Genetic DNA Test
Comprehensive Genetic Analysis for Spinal Development Disorders
The GDF3 Gene Klippel-Feil Syndrome Type 3 Autosomal Dominant NGS Genetic DNA Test represents a cutting-edge diagnostic tool for identifying genetic mutations associated with congenital spinal abnormalities. This specialized test utilizes next-generation sequencing technology to examine the GDF3 gene, which plays a critical role in bone development and vertebral formation during embryonic growth.
What This Test Measures and Detects
Our advanced genetic testing focuses on identifying specific mutations within the GDF3 gene that are responsible for Klippel-Feil syndrome type 3. The test examines:
- Autosomal dominant mutations in the GDF3 gene
- Single nucleotide variants and small insertions/deletions
- Pathogenic variants affecting bone morphogenetic protein signaling
- Genetic alterations impacting vertebral segmentation and development
Who Should Consider This Genetic Test
This specialized DNA test is recommended for individuals presenting with:
- Limited neck mobility and range of motion
- Short neck appearance and low posterior hairline
- Congenital fusion of cervical vertebrae
- Family history of Klippel-Feil syndrome or spinal abnormalities
- Associated symptoms including hearing loss, scoliosis, or renal anomalies
- Unexplained congenital spinal deformities
Clinical Benefits of Genetic Testing
Undergoing the GDF3 gene test provides numerous advantages for patients and healthcare providers:
- Accurate Diagnosis: Confirms or rules out genetic causes of spinal abnormalities
- Family Planning Guidance: Provides crucial information for genetic counseling
- Treatment Planning: Helps orthopedic specialists develop targeted intervention strategies
- Early Intervention: Enables proactive management of associated complications
- Genetic Risk Assessment: Determines inheritance patterns for family members
Understanding Your Test Results
Our comprehensive genetic analysis provides clear, actionable results:
- Positive Result: Indicates the presence of a pathogenic GDF3 gene mutation, confirming Klippel-Feil syndrome type 3 diagnosis
- Negative Result: Suggests no detectable mutation in the GDF3 gene, though other genetic causes may require investigation
- Variant of Uncertain Significance: Identifies genetic changes with unknown clinical impact, requiring further evaluation
All results include detailed interpretation by our certified genetic counselors, who provide personalized guidance on next steps and management strategies.
Test Pricing Information
| Test Component | Price (USD) |
|---|---|
| Discount Price | $500 |
| Regular Price | $700 |
Nationwide Testing Availability
We proudly serve patients 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, San Jose, and many other cities. Our network of certified collection centers ensures accessible genetic testing services nationwide.
Take the Next Step Toward Genetic Clarity
If you or a family member are experiencing symptoms of Klippel-Feil syndrome or have concerns about spinal development abnormalities, our GDF3 genetic test provides the answers you need. Our team of genetic specialists is ready to guide you through the testing process and help you understand your results.
Call us today at +1(267) 388-9828 to schedule your genetic counseling session and book your test appointment. Take control of your genetic health with comprehensive, accurate DNA analysis from America’s leading genetics laboratory.
