LARS2 Gene Hydrops, Lactic Acidosis and Sideroblastic Anemia NGS Genetic DNA Test
Comprehensive Genetic Analysis for Mitochondrial Disorders
The LARS2 Gene Hydrops, Lactic Acidosis and Sideroblastic Anemia NGS Genetic DNA Test represents a cutting-edge diagnostic approach for identifying mutations in the LARS2 gene, which plays a critical role in mitochondrial protein synthesis. This specialized genetic test provides essential insights into complex mitochondrial disorders that affect multiple organ systems, enabling accurate diagnosis and personalized treatment strategies.
What Does This Test Measure?
This advanced genetic test utilizes next-generation sequencing (NGS) technology to comprehensively analyze the entire coding region of the LARS2 gene. The test specifically detects:
- Pathogenic variants in the LARS2 gene encoding mitochondrial leucyl-tRNA synthetase
- Mutations affecting mitochondrial translation and energy production
- Genetic alterations responsible for impaired oxidative phosphorylation
- Variants associated with Perrault syndrome and related mitochondrial disorders
Who Should Consider This Test?
Clinical Indications and Symptoms
This genetic test is recommended for individuals presenting with:
- Unexplained lactic acidosis and metabolic disturbances
- Sideroblastic anemia unresponsive to conventional treatments
- Hydrops fetalis or congenital abnormalities
- Sensorineural hearing loss with systemic symptoms
- Developmental delays and neurological manifestations
- Family history of mitochondrial disorders
- Unexplained multi-organ system dysfunction
Benefits of LARS2 Genetic Testing
Undergoing this comprehensive genetic analysis provides numerous clinical advantages:
- Accurate Diagnosis: Precise identification of LARS2 gene mutations enables definitive diagnosis
- Personalized Treatment: Results guide targeted therapeutic interventions and management strategies
- Genetic Counseling: Provides essential information for family planning and recurrence risk assessment
- Early Intervention: Facilitates timely management of metabolic and hematological complications
- Prognostic Information: Helps predict disease progression and potential complications
Understanding Your Test Results
Interpretation Guidelines
Our comprehensive genetic report includes detailed analysis and interpretation:
- Positive Result: Identifies pathogenic variants in LARS2 gene confirming diagnosis
- Negative Result: No disease-causing mutations detected in analyzed regions
- Variant of Uncertain Significance: Identifies genetic changes requiring further investigation
- Carrier Status: Determines if individuals carry single copies of mutated genes
All results are accompanied by detailed clinical correlations and recommendations from our board-certified genetic specialists.
Test Information and Pricing
| Test Component | Details |
|---|---|
| Test Name | LARS2 Gene Hydrops, Lactic Acidosis and Sideroblastic Anemia 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 |
Nationwide Testing Availability
General Genetics Corporation provides comprehensive genetic testing services across the United States. We have conveniently located branches in all major cities including New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, and San Jose. Our nationwide network ensures accessible genetic testing services for patients throughout the country.
Take Control of Your Genetic Health Today
Don’t let uncertainty about genetic conditions affect your health decisions. Our specialized LARS2 genetic testing provides the clarity you need for informed medical management. With advanced NGS technology and expert genetic analysis, we deliver accurate results that can transform your healthcare journey.
Ready to schedule your genetic test? Contact our genetic specialists today:
Call or WhatsApp: +1(267) 388-9828
Our dedicated team is available to answer your questions, provide pre-test genetic counseling, and help you schedule your appointment at a location convenient for you. Take the first step toward genetic clarity and personalized healthcare management.
