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CST3 Gene Cerebral Amyloid Angiopathy Genetic Test

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

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The CST3 Gene Cerebral Amyloid Angiopathy NGS Genetic DNA Test is a cutting-edge diagnostic tool that identifies mutations in the CST3 gene associated with hereditary cerebral amyloid angiopathy. This comprehensive test utilizes Next-Generation Sequencing (NGS) technology to detect specific genetic variations that can lead to the accumulation of amyloid proteins in cerebral blood vessels, potentially causing strokes, cognitive decline, and neurological complications. Individuals with family history of cerebral amyloid angiopathy, unexplained strokes at young age, or progressive neurological symptoms should consider this test. The test provides crucial information for early intervention, personalized treatment strategies, and family planning decisions. Results are typically available within 3-4 weeks from blood or DNA samples. This advanced genetic testing is available for $500 USD, offering significant savings from the regular $700 USD price.

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CST3 Gene Cerebral Amyloid Angiopathy NGS Genetic DNA Test

Understanding Cerebral Amyloid Angiopathy and CST3 Gene Testing

Cerebral amyloid angiopathy (CAA) represents a serious neurological condition characterized by the accumulation of amyloid proteins in the walls of cerebral blood vessels. The CST3 Gene Cerebral Amyloid Angiopathy NGS Genetic DNA Test provides advanced diagnostic capabilities for identifying hereditary forms of this condition, offering crucial insights for patients and healthcare providers seeking to understand genetic predisposition to cerebrovascular disorders.

What Does This Test Measure?

This comprehensive genetic analysis specifically targets the CST3 gene, which encodes cystatin C – a protein that plays a vital role in regulating amyloid deposition in cerebral vessels. Through Next-Generation Sequencing (NGS) technology, the test identifies:

  • Pathogenic mutations in the CST3 gene associated with hereditary cerebral amyloid angiopathy
  • Specific genetic variants that may increase susceptibility to cerebrovascular complications
  • Inheritance patterns that could affect multiple family generations
  • Genetic markers that influence treatment response and disease progression

Who Should Consider CST3 Gene Testing?

Clinical Indications and Symptoms

This genetic test is particularly recommended for individuals experiencing:

  • Recurrent cerebral hemorrhages or unexplained strokes, especially at younger ages
  • Family history of cerebral amyloid angiopathy or early-onset cerebrovascular disease
  • Progressive cognitive decline with vascular components
  • Unexplained neurological symptoms in individuals with known CST3 gene mutations in family members
  • Patients planning family who have concerns about hereditary neurological conditions

Comprehensive Benefits of CST3 Genetic Testing

Undergoing CST3 gene analysis provides multiple significant advantages:

  • Early Risk Assessment: Identify genetic predisposition before symptom onset
  • Personalized Treatment Planning: Tailor medical interventions based on genetic profile
  • Family Planning Guidance: Make informed decisions about genetic inheritance risks
  • Proactive Monitoring: Implement appropriate surveillance strategies for at-risk individuals
  • Differential Diagnosis: Distinguish hereditary CAA from other cerebrovascular conditions

Understanding Your Test Results

Interpretation Guidance

Your CST3 gene test results will fall into several categories with distinct implications:

  • Positive Result: Indicates the presence of a known pathogenic mutation associated with hereditary cerebral amyloid angiopathy, requiring comprehensive neurological follow-up and family screening
  • Negative Result: Suggests absence of tested CST3 mutations, though does not completely eliminate risk of developing cerebral amyloid angiopathy through other mechanisms
  • Variant of Uncertain Significance: Identifies genetic changes whose clinical significance requires further investigation and periodic re-evaluation
  • Carrier Status: For autosomal recessive forms, indicates carrying one copy of a mutation without disease manifestation

Test Details and Pricing

Test Component Details
Test Name CST3 Gene Cerebral Amyloid Angiopathy 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
Specialty Neurology and Genetics

Pre-Test Requirements and Preparation

To ensure optimal testing outcomes, we recommend:

  • Complete clinical history documentation of the patient undergoing testing
  • Genetic counseling session to develop comprehensive family pedigree chart
  • Discussion of potential implications for family members
  • Understanding of insurance coverage and potential out-of-pocket costs

Nationwide Accessibility

General Genetics Corporation provides CST3 Gene Cerebral Amyloid Angiopathy testing services across the United States, with convenient locations in major metropolitan areas including New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, and San Jose. Our network of certified genetic counselors and neurological specialists ensures comprehensive support throughout your testing journey.

Take Control of Your Neurological Health

Don’t let uncertainty about hereditary cerebral amyloid angiopathy impact your quality of life. Our advanced CST3 gene testing provides the clarity needed for informed healthcare decisions and proactive management of neurological risks.

Ready to schedule your CST3 Gene Cerebral Amyloid Angiopathy NGS Genetic DNA Test? Contact our genetic specialists today at +1(267) 388-9828 or book your appointment online to take the first step toward understanding your genetic predisposition to cerebrovascular health.

Our dedicated team is available to answer your questions, discuss insurance coverage options, and guide you through the testing process with compassion and expertise. Early detection through genetic testing can significantly impact treatment outcomes and quality of life for individuals at risk for hereditary cerebral amyloid angiopathy.