CAT Gene Acatalasemia NGS Genetic DNA Test
Comprehensive Genetic Testing for Acatalasemia Detection
The CAT Gene Acatalasemia NGS Genetic DNA Test represents a breakthrough in genetic diagnostics for metabolic disorders. This advanced testing methodology provides precise detection of mutations in the CAT gene, which encodes the catalase enzyme essential for cellular protection against oxidative stress. Acatalasemia, though rare, can have significant health implications, making early detection through our state-of-the-art NGS technology crucial for proactive healthcare management.
What Does This Test Measure and Detect?
Our comprehensive genetic analysis specifically targets:
- Complete sequencing of the CAT gene using Next-Generation Sequencing technology
- Identification of point mutations, deletions, and insertions affecting catalase production
- Detection of genetic variants associated with impaired hydrogen peroxide metabolism
- Assessment of enzyme deficiency levels through genetic markers
- Evaluation of inherited patterns and carrier status determination
Who Should Consider This Genetic Test?
This test is particularly recommended for individuals experiencing:
- Recurrent oral ulcers and gum infections
- Family history of acatalasemia or related metabolic disorders
- Unexplained oxidative stress symptoms
- Planning for pregnancy with family history of metabolic conditions
- Diagnostic confirmation for suspected catalase deficiency
- Children with developmental delays and oral health issues
Significant Benefits of CAT Gene Testing
Choosing our CAT Gene Acatalasemia NGS Genetic DNA Test provides numerous advantages:
- Early Diagnosis: Enables proactive management before severe symptoms develop
- Personalized Treatment: Guides targeted therapeutic approaches based on genetic profile
- Family Planning: Provides crucial information for genetic counseling and reproductive decisions
- Comprehensive Analysis: NGS technology ensures thorough genetic variant detection
- Professional Support: Includes genetic counseling sessions for result interpretation
- Peace of Mind: Clarifies genetic status and reduces uncertainty about health risks
Understanding Your Test Results
Our genetic specialists provide comprehensive guidance for interpreting your results:
- Normal Results: No detected mutations in the CAT gene, indicating typical catalase function
- Carrier Status: Identification of one mutated gene copy with reduced catalase activity
- Affected Status: Detection of mutations in both CAT gene copies confirming acatalasemia
- Variant of Unknown Significance: Rare genetic changes requiring further clinical correlation
All results include detailed explanations and recommendations for follow-up care with our genetic counseling team.
Test Pricing and Availability
| Test Name | Discount Price | Regular Price |
|---|---|---|
| CAT Gene Acatalasemia NGS Genetic DNA Test | $500 USD | $700 USD |
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, San Jose, and many more. Our network of certified genetic testing facilities ensures accessibility and convenience for patients nationwide.
Take Control of Your Genetic Health Today
Don’t let uncertainty about genetic health risks affect your quality of life. Our CAT Gene Acatalasemia NGS Genetic DNA Test provides the clarity and information you need for informed healthcare decisions. With our discounted price of $500 USD and comprehensive genetic counseling support, you can take proactive steps toward better health management.
Call us now at +1(267) 388-9828 to schedule your genetic test or book your appointment online. Our genetic specialists are ready to assist you with personalized care and professional guidance throughout your testing journey.
Note: Turnaround time for results is 3-4 weeks. Sample types accepted include blood, extracted DNA, or one drop of blood on FTA card. Pre-test requirements include providing clinical history and participating in a genetic counseling session to create a family pedigree chart.
