FOXRED1 Gene Leigh Syndrome NGS Genetic DNA Test
Comprehensive Genetic Testing for Mitochondrial Disorders
The FOXRED1 Gene Leigh Syndrome NGS Genetic DNA Test represents a cutting-edge diagnostic approach for identifying mutations associated with Leigh syndrome, a progressive neurological disorder affecting the central nervous system. This sophisticated genetic analysis utilizes next-generation sequencing technology to provide comprehensive evaluation of the FOXRED1 gene, which plays a critical role in mitochondrial function and energy production within cells.
What Does This Test Measure and Detect?
This advanced genetic test specifically targets the FOXRED1 gene, which encodes a protein essential for the proper assembly and function of mitochondrial complex I. The test detects:
- Pathogenic variants and mutations in the FOXRED1 gene
- Single nucleotide variants (SNVs) and small insertions/deletions
- Genetic alterations that disrupt mitochondrial complex I assembly
- Inheritance patterns of FOXRED1-related Leigh syndrome
- Carrier status for at-risk family members
Who Should Consider This Genetic Test?
This test is recommended for individuals presenting with symptoms suggestive of Leigh syndrome or mitochondrial disorders, including:
- Infants and children with developmental regression or delay
- Patients experiencing neurological symptoms such as seizures, ataxia, or dystonia
- Individuals with elevated lactate levels in blood or cerebrospinal fluid
- Patients with characteristic brain imaging findings of bilateral basal ganglia lesions
- Those with family history of mitochondrial disorders or unexplained infant deaths
- Individuals with progressive neurological deterioration despite standard treatments
Key Benefits of FOXRED1 Genetic Testing
Undergoing this comprehensive genetic analysis provides numerous advantages for patients and families:
- Accurate Diagnosis: Confirms or rules out FOXRED1-related Leigh syndrome with high precision
- Treatment Guidance: Helps clinicians develop targeted management strategies
- Genetic Counseling: Enables informed family planning decisions
- Early Intervention: Facilitates timely implementation of supportive therapies
- Prognostic Information: Provides insights into disease progression and expected outcomes
- Research Contribution: Advances understanding of mitochondrial disorders
Understanding Your Test Results
Your genetic test results will be carefully interpreted by our team of certified genetic counselors and neurologists. Possible outcomes include:
- Positive Result: Identification of pathogenic variants confirms FOXRED1-related Leigh syndrome diagnosis
- Negative Result: No disease-causing variants detected in the FOXRED1 gene
- Variant of Uncertain Significance: Genetic changes with unclear clinical implications requiring further evaluation
- Carrier Status: Identification of individuals who carry one copy of a mutated gene
All results are accompanied by comprehensive explanations and recommendations for next steps, including potential additional testing or clinical management strategies.
Test Pricing and Availability
| Test Component | Price (USD) |
|---|---|
| Discount Price | $500 |
| Regular Price | $700 |
Nationwide Testing Availability
We have diagnostic centers conveniently located across the United States, serving major metropolitan areas 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 testing standards nationwide.
Take Action Today
Don’t let uncertainty about neurological symptoms delay proper diagnosis and treatment. Our team of genetic specialists is ready to help you navigate this complex genetic landscape. Contact us today to schedule your FOXRED1 Gene Leigh Syndrome NGS Genetic DNA Test and take the first step toward clarity and comprehensive care.
Call or WhatsApp us now at +1(267) 388-9828 to book your appointment or discuss your testing options with our genetic counseling team.
