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APOC2 Gene Apolipoprotein CII Deficiency Genetic Test

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

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The APOC2 Gene Apolipoprotein CII Deficiency NGS Genetic DNA Test is a comprehensive genetic analysis that identifies mutations in the APOC2 gene responsible for Apolipoprotein C-II deficiency, a rare inherited metabolic disorder affecting lipid metabolism. This advanced next-generation sequencing test provides precise detection of genetic variants that disrupt normal triglyceride processing, leading to severe hypertriglyceridemia and associated health complications. The test is essential for individuals with unexplained high triglyceride levels, recurrent pancreatitis episodes, or family history of lipid disorders. Results offer crucial insights for accurate diagnosis, personalized treatment strategies, and family planning decisions. Available for only $500 USD, this test provides definitive answers for patients and healthcare providers managing complex metabolic conditions.

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APOC2 Gene Apolipoprotein CII Deficiency NGS Genetic DNA Test

Comprehensive Genetic Analysis for Metabolic Health

The APOC2 Gene Apolipoprotein CII Deficiency NGS Genetic DNA Test represents a cutting-edge diagnostic approach for identifying inherited metabolic disorders affecting lipid metabolism. This sophisticated genetic analysis utilizes next-generation sequencing technology to examine the APOC2 gene, which encodes apolipoprotein C-II – a crucial protein component of triglyceride-rich lipoproteins. Apolipoprotein C-II deficiency is a rare autosomal recessive disorder that significantly impacts the body’s ability to process dietary fats, leading to potentially severe health consequences when left undiagnosed.

What This Advanced Genetic Test Detects

This comprehensive NGS-based genetic test specifically targets mutations within the APOC2 gene that disrupt normal apolipoprotein C-II function. The test identifies:

  • Pathogenic variants affecting lipoprotein lipase activation
  • Genetic mutations causing impaired triglyceride clearance
  • Inherited defects in lipid metabolism pathways
  • Specific nucleotide changes affecting protein structure and function
  • Both known and novel genetic variants associated with Apolipoprotein C-II deficiency

Who Should Consider This Genetic Test

This specialized genetic analysis is recommended for individuals presenting with specific clinical indications:

  • Patients with persistently elevated triglyceride levels unresponsive to conventional treatments
  • Individuals experiencing recurrent episodes of acute pancreatitis
  • Those with family history of inherited lipid disorders or metabolic conditions
  • Patients displaying xanthomas (cholesterol deposits in skin)
  • Individuals with hepatosplenomegaly (enlarged liver and spleen)
  • Children or adults with unexplained abdominal pain and lipid abnormalities
  • Patients requiring definitive diagnosis for appropriate therapeutic interventions

Significant Benefits of Genetic Testing

Undergoing the APOC2 Gene Apolipoprotein CII Deficiency NGS Genetic DNA Test provides numerous clinical advantages:

  • Accurate Diagnosis: Provides definitive identification of genetic causes behind metabolic symptoms
  • Personalized Treatment: Enables targeted therapeutic approaches based on genetic findings
  • Family Planning: Offers crucial information for genetic counseling and reproductive decisions
  • Early Intervention: Facilitates proactive management to prevent complications
  • Comprehensive Analysis: Utilizes advanced NGS technology for thorough genetic assessment
  • Clinical Guidance: Supports healthcare providers in developing effective treatment strategies

Understanding Your Genetic Test Results

Test results provide detailed genetic information that requires professional interpretation:

  • Positive Result: Indicates presence of pathogenic variants in APOC2 gene, confirming diagnosis of Apolipoprotein C-II deficiency
  • Negative Result: Suggests absence of known disease-causing mutations in the APOC2 gene
  • Variant of Uncertain Significance: Identifies genetic changes with unclear clinical implications requiring further evaluation
  • Carrier Status: Detects individuals with one mutated copy who may pass the condition to offspring

All results should be discussed with a qualified genetic counselor or metabolic specialist to ensure proper understanding and appropriate clinical management.

Test Pricing and Availability

Test Name Discount Price Regular Price
APOC2 Gene Apolipoprotein CII Deficiency NGS Genetic DNA Test $500 USD $700 USD

Nationwide Testing Accessibility

We maintain comprehensive testing facilities across the United States, with convenient locations in all major metropolitan areas including New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, San Jose, and numerous other cities. Our network ensures accessible genetic testing services for patients throughout the country.

Schedule Your Genetic Assessment Today

Take the first step toward understanding your genetic health and managing metabolic conditions effectively. Our experienced genetic counselors and metabolic specialists are available to guide you through the testing process and interpret your results. Contact us today to schedule your APOC2 Gene Apolipoprotein CII Deficiency NGS Genetic DNA Test and gain valuable insights into your metabolic health.

Call or WhatsApp: +1(267) 388-9828 to book your comprehensive genetic analysis and receive professional guidance from our expert team.