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PML/RARA AML M3 APML Genetic Test

Original price was: $176.Current price is: $132.

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The PML/RARA AML M3 APML genetic test is a specialized diagnostic tool for detecting Acute Promyelocytic Leukemia, a specific subtype of acute myeloid leukemia. This test identifies the characteristic chromosomal translocation between chromosomes 15 and 17, which creates the PML/RARA fusion gene responsible for this aggressive blood cancer. Using Fluorescence In Situ Hybridization (FISH) technology, the test provides highly accurate detection of this genetic abnormality in bone marrow or peripheral blood samples. Patients experiencing symptoms like unexplained bleeding, bruising, fatigue, or recurrent infections should consider this test for proper diagnosis. Early detection enables targeted therapy with all-trans retinoic acid (ATRA), significantly improving treatment outcomes. The test costs $132 USD and delivers results within 3-4 days, making it an essential tool for leukemia diagnosis and monitoring treatment response.

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PML/RARA AML M3 APML Genetic Test

Understanding Acute Promyelocytic Leukemia Testing

The PML/RARA AML M3 APML genetic test represents a critical advancement in hematologic oncology diagnostics, specifically designed to detect Acute Promyelocytic Leukemia (APL), classified as AML-M3 in the French-American-British classification system. This specialized test identifies the unique genetic signature that characterizes this distinct leukemia subtype, enabling precise diagnosis and targeted treatment approaches.

What Does the PML/RARA Test Measure?

This sophisticated genetic analysis detects the specific chromosomal translocation t(15;17), which results in the fusion of the PML (Promyelocytic Leukemia) gene on chromosome 15 with the RARA (Retinoic Acid Receptor Alpha) gene on chromosome 17. This abnormal genetic rearrangement creates the PML/RARA fusion gene, which disrupts normal cellular differentiation and promotes uncontrolled growth of promyelocytes in the bone marrow.

  • Detection of t(15;17) chromosomal translocation
  • Identification of PML/RARA fusion gene expression
  • Confirmation of Acute Promyelocytic Leukemia diagnosis
  • Monitoring of minimal residual disease during treatment
  • Assessment of treatment response and potential relapse

Who Should Consider PML/RARA Testing?

This genetic test is essential for individuals presenting with clinical symptoms suggestive of Acute Promyelocytic Leukemia or those with abnormal blood counts requiring further investigation.

Clinical Indications and Symptoms

  • Unexplained bleeding tendencies or excessive bruising
  • Persistent fatigue and weakness
  • Recurrent infections and fever
  • Abnormal blood counts showing pancytopenia
  • Bone pain or discomfort
  • Unexplained weight loss
  • Enlarged liver or spleen
  • Patients with suspected acute myeloid leukemia

Benefits of PML/RARA Genetic Testing

Early and accurate detection of the PML/RARA fusion gene provides numerous clinical advantages for patients and healthcare providers.

Key Advantages

  • Precise Diagnosis: Confirms APL diagnosis with high specificity
  • Targeted Therapy: Enables treatment with all-trans retinoic acid (ATRA)
  • Improved Outcomes: Early detection significantly increases survival rates
  • Treatment Monitoring: Tracks response to therapy and detects relapse
  • Risk Stratification: Helps determine appropriate treatment intensity
  • Genetic Counseling: Provides valuable information for family planning

Understanding Your Test Results

Interpreting PML/RARA test results requires careful consideration of clinical context and laboratory findings.

Result Interpretation Guidelines

  • Positive Result: Indicates presence of PML/RARA fusion gene, confirming APL diagnosis
  • Negative Result: Suggests absence of the characteristic genetic abnormality
  • Quantitative Results: May indicate the percentage of cells carrying the fusion gene
  • Follow-up Testing: Regular monitoring may be recommended during treatment
  • Clinical Correlation: Results should be interpreted alongside other laboratory findings

Test Information and Pricing

Test Component Details
Test Name PML/RARA AML M3 APML Genetic Test
Regular Price $176 USD
Discount Price $132 USD
Turnaround Time 3-4 Days
Sample Type Bone Marrow / Peripheral Blood
Test Components Sodium Heparin Vacutainer (2ml)
Methodology FISH (Fluorescence In Situ Hybridization)

Nationwide Testing Availability

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, and San Jose. Our state-of-the-art facilities ensure consistent, high-quality testing services nationwide.

Book Your Genetic Test Today

Take the first step toward accurate leukemia diagnosis and personalized treatment. Our experienced genetic counselors and oncology specialists are ready to assist you with comprehensive testing and result interpretation.

Call or WhatsApp us today at +1(267) 388-9828 to schedule your PML/RARA AML M3 APML genetic test. Early detection saves lives, and our rapid 3-4 day turnaround ensures you receive critical diagnostic information when you need it most.

Important Pre-Test Information

The PML/RARA AML M3 APML genetic test requires a physician’s prescription for diagnostic purposes. Please note that prescriptions are not applicable for surgical procedures, pregnancy cases, or individuals planning international travel. Consult with your healthcare provider to determine if this test is appropriate for your clinical situation.