MT-TC Gene MELAS Syndrome NGS Genetic DNA Test
Comprehensive Mitochondrial Disorder Detection
The MT-TC Gene MELAS Syndrome NGS Genetic DNA Test represents a breakthrough in mitochondrial disease diagnostics, offering unparalleled accuracy in detecting mutations responsible for Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-like episodes (MELAS) syndrome. This advanced genetic screening utilizes state-of-the-art Next-Generation Sequencing technology to identify specific mutations in the MT-TC gene that can lead to severe neurological and metabolic complications.
What Does This Test Measure?
This comprehensive genetic analysis specifically targets the MT-TC gene, which encodes for transfer RNA that plays a critical role in mitochondrial protein synthesis. The test detects:
- Point mutations in the MT-TC mitochondrial DNA
- Genetic variations associated with MELAS syndrome
- Heteroplasmy levels (mixture of mutant and normal mitochondrial DNA)
- Specific mutations known to cause mitochondrial dysfunction
Who Should Consider This Test?
This genetic screening is recommended for individuals experiencing symptoms suggestive of mitochondrial disorders, including:
- Recurrent stroke-like episodes in young adults
- Progressive neurological deterioration
- Muscle weakness and exercise intolerance
- Seizures or epilepsy of unknown origin
- Developmental delays in children
- Family history of mitochondrial diseases
- Unexplained lactic acidosis
- Vision or hearing problems of mitochondrial origin
Key Benefits of MT-TC Gene Testing
Early detection through this advanced genetic test provides numerous advantages:
- Accurate diagnosis enabling targeted treatment approaches
- Early intervention to prevent disease progression
- Family planning guidance and genetic counseling
- Personalized management strategies for mitochondrial disorders
- Reduced diagnostic uncertainty and medical costs
- Improved quality of life through appropriate therapeutic interventions
Understanding Your Test Results
Your genetic test results will be thoroughly explained by our certified genetic counselors. Positive results indicate the presence of MT-TC gene mutations associated with MELAS syndrome, requiring comprehensive medical management. Negative results suggest the absence of tested mutations, though additional testing may be recommended based on clinical presentation. Variants of uncertain significance may require further evaluation and family studies.
Test Details and Pricing
| Test Component | Details |
|---|---|
| Test Name | MT-TC Gene MELAS 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 |
| Specialty | Cardiology, Genetics |
| Testing Method | NGS Technology |
Pre-Test Requirements
Before scheduling your test, please ensure you have:
- Complete clinical history documentation
- Scheduled genetic counseling session
- Family pedigree chart for affected relatives
- Relevant medical records and previous test results
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 more cities. Our network of certified laboratories ensures consistent, high-quality testing standards nationwide.
Take Control of Your Health Today
Don’t let uncertainty about mitochondrial disorders affect your quality of life. Early detection through the MT-TC Gene MELAS Syndrome NGS Genetic DNA Test can provide the answers you need for proper diagnosis and management. Our team of genetic specialists is ready to guide you through the testing process and help you understand your results.
Call or WhatsApp us today at +1(267) 388-9828 to schedule your genetic counseling session and book your test. Take the first step toward clarity and personalized healthcare management.
