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ACADS Gene Acyl-CoA Short-Chain Dehydrogenase Deficiency Genetic Test

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

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The ACADS Gene Acyl-CoA Short-Chain Dehydrogenase Deficiency NGS Genetic DNA Test is a comprehensive genetic screening that identifies mutations in the ACADS gene responsible for short-chain acyl-CoA dehydrogenase deficiency (SCADD). This inherited metabolic disorder affects the body’s ability to break down certain fats for energy, potentially leading to serious health complications if undiagnosed. Using advanced Next-Generation Sequencing (NGS) technology, this test provides precise detection of genetic variants associated with SCADD. The test is particularly important for individuals with unexplained metabolic symptoms, developmental delays, or family history of metabolic disorders. Early detection through this $500 USD test enables proactive management and preventive care strategies. Results are typically available within 3-4 weeks from blood sample collection. Genetic counseling is recommended before testing to understand family inheritance patterns.

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ACADS Gene Acyl-CoA Short-Chain Dehydrogenase Deficiency NGS Genetic DNA Test

Comprehensive Introduction to ACADS Genetic Testing

The ACADS Gene Acyl-CoA Short-Chain Dehydrogenase Deficiency NGS Genetic DNA Test represents a breakthrough in metabolic disorder diagnostics. This advanced genetic screening utilizes cutting-edge Next-Generation Sequencing (NGS) technology to identify mutations in the ACADS gene, which plays a critical role in fatty acid metabolism. Short-chain acyl-CoA dehydrogenase deficiency (SCADD) is an inherited metabolic condition that can lead to significant health challenges if left undiagnosed and untreated.

This test is particularly vital because SCADD affects the body’s ability to convert certain fats into energy, potentially causing metabolic crises, developmental delays, and neurological symptoms. Early detection through comprehensive genetic testing enables healthcare providers to implement preventive strategies and personalized treatment plans, significantly improving patient outcomes and quality of life.

What This Test Measures and Detects

The ACADS Gene NGS Genetic DNA Test specifically analyzes:

  • Complete sequencing of the ACADS gene to identify pathogenic variants
  • Mutations affecting short-chain acyl-CoA dehydrogenase enzyme function
  • Genetic markers associated with impaired fatty acid oxidation
  • Inheritance patterns of SCADD within families
  • Risk assessment for metabolic complications

Using state-of-the-art NGS technology, this test provides comprehensive coverage of the ACADS gene, ensuring high accuracy in detecting both common and rare genetic variants that contribute to short-chain acyl-CoA dehydrogenase deficiency.

Who Should Consider This Genetic Test

Clinical Indications and Symptoms

This test is recommended for individuals experiencing:

  • Unexplained metabolic acidosis or hypoglycemia
  • Developmental delays or neurological abnormalities
  • Muscle weakness or exercise intolerance
  • Family history of metabolic disorders
  • Unexplained seizures or epilepsy
  • Feeding difficulties in infants
  • Failure to thrive in childhood
  • Recurrent vomiting or lethargy

High-Risk Populations

  • Newborns with abnormal newborn screening results
  • Children with unexplained developmental concerns
  • Adults with metabolic symptoms
  • Individuals with family history of SCADD
  • Couples planning pregnancy with metabolic disorder concerns

Significant Benefits of ACADS Genetic Testing

Undergoing the ACADS Gene NGS Genetic DNA Test provides numerous advantages:

  • Early Diagnosis: Enables prompt intervention before serious complications develop
  • Personalized Treatment: Guides dietary modifications and medical management
  • Family Planning: Provides crucial information for reproductive decisions
  • Preventive Care: Helps avoid metabolic crises through proactive management
  • Peace of Mind: Reduces uncertainty about unexplained symptoms
  • Comprehensive Analysis: NGS technology ensures thorough genetic assessment

Understanding Your Test Results

Interpretation Guidelines

Your ACADS genetic test results will fall into one of several categories:

  • Positive Result: Indicates the presence of pathogenic variants in the ACADS gene, confirming SCADD diagnosis
  • Negative Result: No disease-causing mutations detected, though clinical correlation is essential
  • Variant of Uncertain Significance (VUS): Genetic changes with unknown clinical impact requiring further evaluation
  • Carrier Status: Identification of individuals who carry one copy of a mutated gene

Next Steps After Testing

Following your test results, our genetic counseling team will:

  • Provide comprehensive result interpretation
  • Discuss implications for family members
  • Recommend appropriate follow-up care
  • Coordinate with your healthcare provider for management planning
  • Offer ongoing support and resources

Test Pricing and Booking Information

Test Component Price (USD)
Discount Price $500
Regular Price $700
Turnaround Time 3 to 4 Weeks
Sample Type Blood

Nationwide Testing Availability

GGC DNA provides comprehensive genetic testing services across the United States, with convenient locations in all major cities including New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, and San Jose. Our state-of-the-art laboratories ensure consistent, high-quality results regardless of your location.

Take Action Today

Don’t let uncertainty about metabolic health concerns affect your quality of life. The ACADS Gene Acyl-CoA Short-Chain Dehydrogenase Deficiency NGS Genetic DNA Test provides the clarity and information needed for informed healthcare decisions. Our experienced genetic counselors are available to discuss your testing options and answer any questions.

Book your test today by calling +1(267) 388-9828 or visiting our website to schedule your appointment. Take the first step toward understanding your genetic health and ensuring optimal metabolic wellness for you and your family.

Remember: Early detection through genetic testing can significantly improve outcomes for individuals with metabolic disorders. Trust GGC DNA for accurate, reliable genetic testing backed by cutting-edge technology and expert medical guidance.