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CBFB-MYH11 Inv(16) Qualitative Test

Original price was: $150.Current price is: $112.

-25%

The CBFB-MYH11 Inv(16) Qualitative test is a sophisticated genetic diagnostic tool designed to detect the specific chromosomal inversion associated with acute myeloid leukemia (AML). This Real Time PCR-based test identifies the fusion gene created by the inversion between chromosomes 16p13 and 16q22, which is crucial for diagnosing and monitoring certain subtypes of AML. The test is particularly valuable for patients presenting with symptoms of leukemia, those undergoing treatment monitoring, or individuals requiring genetic confirmation of AML subtype. With results available in just 3-4 days and a discounted price of $112 USD (regularly $150), this test provides essential information for treatment planning and disease management. Available at all GGC DNA locations across major US cities.

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CBFB-MYH11 Inv(16) Qualitative Test

Understanding the CBFB-MYH11 Inv(16) Qualitative Test

The CBFB-MYH11 Inv(16) Qualitative test represents a cutting-edge molecular diagnostic approach for detecting specific genetic abnormalities associated with acute myeloid leukemia (AML). This sophisticated test utilizes Real Time PCR technology to identify the chromosomal inversion between chromosomes 16p13 and 16q22, which creates a fusion gene between the CBFB and MYH11 genes. This genetic alteration is particularly significant as it defines a distinct subtype of AML with unique clinical characteristics and treatment responses.

What This Test Measures and Detects

The CBFB-MYH11 Inv(16) Qualitative test specifically targets and identifies:

  • The presence of the inv(16)(p13q22) chromosomal inversion
  • The CBFB-MYH11 fusion gene transcript
  • Genetic markers associated with core-binding factor acute myeloid leukemia
  • Molecular evidence for AML-M4Eo subtype classification

Who Should Consider This Test

This genetic test is recommended for individuals experiencing:

  • Unexplained fatigue, weakness, or persistent tiredness
  • Frequent infections or unusual susceptibility to illness
  • Unexplained bruising, bleeding, or petechiae
  • Bone pain or tenderness
  • Enlarged lymph nodes, spleen, or liver
  • Abnormal blood cell counts on routine testing
  • Previous diagnosis of AML requiring subtype confirmation
  • Monitoring treatment response in known CBFB-MYH11 positive AML

Clinical Benefits of Testing

Undergoing the CBFB-MYH11 Inv(16) Qualitative test provides numerous advantages:

  • Accurate Diagnosis: Precise identification of AML subtype for targeted treatment planning
  • Prognostic Information: Understanding disease course and expected outcomes
  • Treatment Guidance: Informing chemotherapy and targeted therapy decisions
  • Minimal Residual Disease Monitoring: Tracking treatment effectiveness over time
  • Early Detection: Identifying genetic abnormalities before full disease manifestation
  • Family Planning Insights: Understanding genetic implications for future generations

Understanding Your Test Results

Your CBFB-MYH11 Inv(16) Qualitative test results will be clearly interpreted by our genetic specialists:

  • Positive Result: Indicates the presence of the CBFB-MYH11 fusion gene, confirming inv(16) associated AML
  • Negative Result: Suggests absence of this specific genetic abnormality, though other AML subtypes may still be present
  • Quantitative Values: When applicable, provides information about mutation burden for monitoring purposes

All results are accompanied by comprehensive explanations and recommendations for next steps. Our genetic counselors are available to discuss your results and answer any questions you may have about their implications for your health and treatment options.

Test Details and Pricing

Test Parameter Details
Test Name CBFB-MYH11 Inv(16) Qualitative
Regular Price $150 USD
Discount Price $112 USD
Turnaround Time 3-4 Days
Sample Type Bone Marrow / Peripheral Blood (Transport Immediately)
Test Components EDTA Vacutainer (2ml)
Testing Method Real Time PCR
Specialty General Physician

Pre-Test Instructions and Requirements

The CBFB-MYH11 Inv(16) Qualitative test requires a Doctor’s prescription for most cases. However, prescription requirements do not apply for:

  • Surgical preparation cases
  • Pregnancy-related testing
  • Individuals planning international travel requiring medical documentation

For all other circumstances, please consult with your healthcare provider to obtain the necessary prescription before scheduling your test.

Nationwide Availability

GGC DNA has testing facilities conveniently located across the United States, serving patients in all major metropolitan areas including:

  • New York City and surrounding regions
  • Los Angeles and Southern California
  • Chicago and the Midwest
  • Houston, Dallas, and Texas locations
  • Miami and Florida centers
  • Washington D.C. and Baltimore areas
  • San Francisco and Bay Area facilities
  • And many more locations nationwide

Take Control of Your Health Today

Don’t wait to get the critical genetic information you need for proper diagnosis and treatment planning. The CBFB-MYH11 Inv(16) Qualitative test provides essential insights into your genetic health and can significantly impact your treatment journey.

Ready to schedule your test? Contact us today:

Phone: +1(267) 388-9828

WhatsApp: +1(267) 388-9828

Our friendly staff is available to answer your questions, help you understand the testing process, and schedule your appointment at the most convenient location. Take the first step toward comprehensive genetic understanding and personalized medical care.