CTDP1 Gene CMT4 CTDP1 Related NGS Genetic DNA Test
Comprehensive Genetic Testing for Hereditary Neuropathy
The CTDP1 Gene CMT4 CTDP1 Related NGS Genetic DNA Test represents a breakthrough in neurological genetic diagnostics, specifically designed to identify mutations in the CTDP1 gene that cause Charcot-Marie-Tooth disease type 4 (CMT4). This advanced testing methodology provides crucial insights into hereditary neurological conditions affecting peripheral nerves.
What Does This Test Measure?
This sophisticated genetic analysis utilizes Next-Generation Sequencing (NGS) technology to comprehensively examine the CTDP1 gene for specific mutations and variations. The test detects:
- Pathogenic variants in the CTDP1 gene associated with CMT4
- Single nucleotide polymorphisms (SNPs) affecting gene function
- Copy number variations and structural abnormalities
- Inheritance patterns for genetic counseling purposes
Who Should Consider This Test?
This genetic test is recommended for individuals experiencing symptoms or having risk factors for CMT4, including:
- Progressive muscle weakness in hands and feet
- Foot deformities such as high arches or hammertoes
- Reduced sensation in extremities
- Family history of Charcot-Marie-Tooth disease
- Delayed motor development in children
- Difficulty with balance and coordination
- Muscle atrophy in lower legs and hands
Clinical Benefits of Testing
Undergoing the CTDP1 Gene CMT4 test provides numerous advantages for patients and healthcare providers:
- Early Diagnosis: Enables prompt intervention and management strategies
- Family Planning: Provides critical information for genetic counseling
- Personalized Treatment: Guides targeted therapeutic approaches
- Prognostic Information: Helps predict disease progression and severity
- Clinical Trial Eligibility: Opens opportunities for specialized treatments
Understanding Your Test Results
Our comprehensive genetic counseling services help interpret your results with clarity and precision:
- Positive Result: Indicates presence of CTDP1 gene mutation; requires follow-up with neurologist
- Negative Result: No detected mutation; may still require additional testing based on symptoms
- Variant of Uncertain Significance: Requires ongoing monitoring and possible family studies
- Carrier Status: Important information for family planning decisions
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 cities including New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, and San Jose. Our state-of-the-art facilities ensure consistent, high-quality genetic testing services nationwide.
Schedule Your Genetic Test Today
Take the first step toward understanding your neurological health. Our expert genetic counselors and neurologists are ready to provide comprehensive care and support throughout your testing journey.
Call or WhatsApp us today at +1(267) 388-9828 to book your CTDP1 Gene CMT4 CTDP1 Related NGS Genetic DNA Test and receive professional genetic counseling services.
Turnaround Time: 3-4 Weeks | Sample Type: Blood, Extracted DNA, or One Drop Blood on FTA Card
