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ASL Gene Argininosuccinic Aciduria Genetic Test

Original price was: $700.Current price is: $500.

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The ASL Gene Argininosuccinic Aciduria NGS Genetic DNA Test is a cutting-edge diagnostic tool that identifies mutations in the ASL gene responsible for argininosuccinic aciduria, a rare metabolic disorder affecting the urea cycle. This comprehensive test utilizes Next-Generation Sequencing (NGS) technology to provide precise genetic analysis, enabling early detection and intervention for affected individuals. The test is particularly valuable for newborns showing symptoms of hyperammonemia, developmental delays, or unexplained neurological issues. By identifying specific genetic mutations, healthcare providers can develop targeted treatment strategies and provide accurate genetic counseling for family planning. The test costs $500 USD and offers reliable results within 3-4 weeks, using blood samples or extracted DNA for analysis. Early diagnosis through this test can significantly improve patient outcomes and quality of life.

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ASL Gene Argininosuccinic Aciduria NGS Genetic DNA Test

Comprehensive Genetic Testing for Metabolic Disorders

The ASL Gene Argininosuccinic Aciduria NGS Genetic DNA Test represents a breakthrough in genetic diagnostics for metabolic disorders. This advanced test specifically targets mutations in the ASL (argininosuccinate lyase) gene, which plays a critical role in the urea cycle – the body’s primary mechanism for removing toxic ammonia from the bloodstream. When the ASL gene functions improperly, it leads to argininosuccinic aciduria, a serious inherited metabolic condition that can cause life-threatening complications if left undiagnosed.

What This Test Measures and Detects

Our NGS-based genetic test provides comprehensive analysis of the ASL gene to identify pathogenic variants that cause argininosuccinic aciduria. The test specifically detects:

  • Point mutations, deletions, and insertions in the ASL gene
  • Single nucleotide variants (SNVs) affecting enzyme function
  • Copy number variations (CNVs) that may disrupt gene expression
  • Novel genetic variants with potential clinical significance
  • Inheritance patterns through family genetic analysis

Who Should Consider This Test

This genetic test is recommended for individuals displaying symptoms or risk factors associated with urea cycle disorders:

  • Newborns with unexplained hyperammonemia (elevated blood ammonia levels)
  • Infants experiencing feeding difficulties, vomiting, or lethargy
  • Children with developmental delays or neurological symptoms
  • Patients with family history of metabolic disorders
  • Individuals with elevated argininosuccinic acid in urine tests
  • Parents planning pregnancy with known family history of urea cycle disorders
  • Siblings of diagnosed patients for carrier status determination

Key Benefits of ASL Gene Testing

Early genetic testing provides numerous advantages for patients and families:

  • Early Intervention: Enables prompt treatment before serious complications develop
  • Accurate Diagnosis: Provides definitive confirmation of argininosuccinic aciduria
  • Personalized Treatment: Guides dietary management and medication strategies
  • Family Planning: Informs reproductive decisions and genetic counseling
  • Prognostic Information: Helps predict disease severity and progression
  • Preventive Care: Allows monitoring and prevention of metabolic crises

Understanding Your Test Results

Our comprehensive genetic report provides clear, actionable information:

  • Positive Result: Indicates presence of pathogenic ASL gene mutations confirming argininosuccinic aciduria diagnosis
  • Negative Result: Suggests absence of known disease-causing mutations in the ASL gene
  • Variant of Uncertain Significance: Identifies genetic changes with unknown clinical impact requiring further evaluation
  • Carrier Status: Determines if an individual carries one copy of a mutated gene

All results include detailed interpretation by our certified genetic counselors, who provide personalized recommendations for next steps and management strategies.

Test Pricing and Details

Test Feature Details
Test Name ASL Gene Argininosuccinic Aciduria 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

Pre-Test Requirements

To ensure accurate results and comprehensive care, we recommend:

  • Complete clinical history of the patient
  • Genetic counseling session to create family pedigree chart
  • Documentation of affected family members
  • Previous metabolic test results if available

Nationwide Accessibility

We have diagnostic centers conveniently located across the United States, serving patients in all major metropolitan areas including New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, San Jose, and many more. Our network ensures that quality genetic testing is accessible to everyone nationwide.

Take Control of Your Genetic Health Today

Don’t wait for symptoms to escalate. Early detection of argininosuccinic aciduria through ASL gene testing can significantly improve treatment outcomes and quality of life. Our team of genetic specialists and metabolic disorder experts are ready to guide you through the testing process and provide comprehensive support.

Call or WhatsApp us now at +1(267) 388-9828 to schedule your ASL Gene Argininosuccinic Aciduria NGS Genetic DNA Test and take the first step toward understanding your genetic health.

Our dedicated genetic counselors are available to answer your questions, discuss insurance coverage options, and help you prepare for testing. With our state-of-the-art NGS technology and experienced medical team, you can trust General Genetics Corporation for accurate, reliable genetic testing results.