MACF1 Gene Neurodevelopmental Disorder NGS Genetic DNA Test
Comprehensive Genetic Analysis for Neurological Development
The MACF1 Gene Neurodevelopmental Disorder NGS Genetic DNA Test represents a breakthrough in genetic diagnostics for neurological conditions. This advanced test specifically targets the MACF1 (Microtubule-Actin Crosslinking Factor 1) gene, which plays a crucial role in neuronal development and function. Mutations in this gene have been linked to various neurodevelopmental disorders characterized by intellectual disability, developmental delays, and neurological abnormalities.
What Does This Test Measure?
Our NGS-based genetic test provides comprehensive analysis of the MACF1 gene to detect:
- Point mutations and single nucleotide variants
- Small insertions and deletions (indels)
- Copy number variations affecting the MACF1 gene
- Structural variants impacting gene function
- Pathogenic and likely pathogenic variants associated with neurodevelopmental disorders
Who Should Consider This Test?
This genetic test is particularly recommended for individuals presenting with:
- Unexplained developmental delays in childhood
- Intellectual disability of unknown origin
- Neurological symptoms without clear diagnosis
- Family history of neurodevelopmental disorders
- Multiple congenital anomalies with neurological involvement
- Suspected genetic syndromes affecting brain development
- Abnormal brain imaging findings
Key Benefits of MACF1 Genetic Testing
- Accurate Diagnosis: Provides definitive answers for complex neurological conditions
- Personalized Treatment: Enables targeted therapeutic interventions based on genetic findings
- Family Planning: Offers crucial information for genetic counseling and reproductive decisions
- Early Intervention: Facilitates timely support services and educational planning
- Comprehensive Analysis: Utilizes state-of-the-art NGS technology for maximum detection sensitivity
- Medical Management: Guides appropriate medical care and monitoring strategies
Understanding Your Test Results
Your genetic test report will provide detailed information about MACF1 gene variants identified:
- Positive Result: Indicates the presence of a pathogenic variant in the MACF1 gene, confirming the genetic basis of neurodevelopmental symptoms
- Negative Result: Suggests no disease-causing variants were detected in the MACF1 gene, though other genetic causes may need investigation
- Variant of Uncertain Significance (VUS): Identifies genetic changes whose clinical significance is currently unknown, requiring further evaluation
- Carrier Status: May identify individuals who carry one copy of a mutated gene without showing symptoms
Test Details and Pricing
| Test Feature | Details |
|---|---|
| Test Name | MACF1 Gene Neurodevelopmental Disorder 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) Technology |
| Specialty | Neurology and Genetics |
Nationwide Testing Availability
We have diagnostic centers conveniently located across the United States, including major metropolitan areas such as New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, San Jose, and many other cities. Our network of certified genetic testing facilities ensures accessible, reliable testing services nationwide.
Take the Next Step Toward Answers
If you or your loved one is experiencing unexplained neurological symptoms or developmental concerns, the MACF1 Gene Neurodevelopmental Disorder NGS Genetic DNA Test could provide the answers you need. Our genetic counselors and neurological specialists are available to discuss your specific situation and determine if this test is appropriate for your needs.
Call or WhatsApp us today at +1(267) 388-9828 to schedule your genetic counseling session and book your MACF1 genetic test. Take control of your neurological health with definitive genetic insights from America’s leading genetics laboratory.
