NBAS Gene Infantile Liver Failure Syndrome Type 2 NGS Genetic DNA Test
Comprehensive Genetic Testing for Pediatric Liver Disorders
The NBAS Gene Infantile Liver Failure Syndrome Type 2 NGS Genetic DNA Test represents a breakthrough in pediatric genetic diagnostics, specifically designed to identify mutations in the NBAS gene that cause infantile liver failure syndrome type 2. This rare genetic disorder affects infants and young children, leading to severe liver dysfunction and potentially life-threatening complications if not diagnosed early.
What This Advanced Genetic Test Detects
Our state-of-the-art NGS (Next-Generation Sequencing) technology precisely analyzes the NBAS gene to identify pathogenic variants associated with infantile liver failure syndrome type 2. The test examines:
- Point mutations and small insertions/deletions in the NBAS gene
- Copy number variations affecting gene function
- Specific genetic markers linked to liver dysfunction
- Inheritance patterns and carrier status
Who Should Consider This Genetic Test
This specialized genetic testing is recommended for infants and children presenting with:
- Unexplained acute liver failure in infancy
- Recurrent episodes of liver dysfunction
- Failure to thrive and developmental delays
- Family history of infantile liver disorders
- Metabolic abnormalities without clear cause
- Suspected genetic liver conditions
Significant Benefits of Early Genetic Diagnosis
Early detection through NBAS gene testing provides numerous advantages:
- Timely Intervention: Enables prompt medical management and treatment planning
- Family Planning: Provides crucial information for genetic counseling and future family planning
- Personalized Care: Facilitates tailored treatment approaches based on genetic findings
- Prognostic Insights: Helps predict disease progression and potential complications
- Peace of Mind: Reduces diagnostic uncertainty for families and healthcare providers
Understanding Your Test Results
Our comprehensive genetic report includes detailed analysis and interpretation:
- Positive Result: Indicates the presence of pathogenic NBAS gene mutations, confirming the diagnosis of infantile liver failure syndrome type 2
- Negative Result: Suggests no detectable mutations in the NBAS gene, though other genetic causes may need investigation
- Variant of Uncertain Significance: Identifies genetic changes whose clinical significance requires further evaluation
- Carrier Status: Determines if individuals carry one copy of the mutated gene without showing symptoms
All results are accompanied by detailed genetic counseling to ensure proper understanding and appropriate next steps.
Test Pricing and Details
| Test Feature | Details |
|---|---|
| Test Name | NBAS Gene Infantile Liver Failure Syndrome Type 2 NGS Genetic DNA Test |
| Regular Price | $700 USD |
| Discount Price | $500 USD |
| Turnaround Time | 3 to 4 Weeks |
| Sample Type | Blood, Extracted DNA, or One Drop Blood on FTA Card |
| Testing Method | NGS Technology |
Pre-Test Requirements
Before scheduling your NBAS gene test, please ensure:
- Complete clinical history of the patient
- Genetic counseling session to create a detailed family pedigree
- Documentation of affected family members with similar symptoms
- Review of previous medical evaluations and test results
Nationwide Accessibility
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 consistent, high-quality results nationwide.
Take Action Today
Don’t wait to get the answers you need for your child’s health. Early genetic diagnosis can make a significant difference in treatment outcomes and quality of life. Our team of genetic specialists is ready to guide you through the testing process and provide comprehensive support.
Call or WhatsApp us today at +1(267) 388-9828 to schedule your NBAS Gene Infantile Liver Failure Syndrome Type 2 NGS Genetic DNA Test and take the first step toward accurate diagnosis and personalized care.