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Multiplex Fluorescence In Situ Hybridization (mFISH)

Original price was: $750.Current price is: $562.

-25%

Multiplex Fluorescence In Situ Hybridization (mFISH) is an advanced genetic testing method that simultaneously detects multiple chromosomal abnormalities using fluorescent probes. This sophisticated technique provides comprehensive analysis of chromosomal rearrangements, deletions, and duplications that traditional methods might miss. mFISH is particularly valuable for cancer diagnosis, monitoring treatment response, and identifying complex genetic disorders. The test analyzes bone marrow or peripheral blood samples using specialized fluorescent probes that bind to specific chromosomal regions. With results available in 10-15 days, mFISH offers clinicians critical information for personalized treatment planning and genetic counseling. This test is available for $562 USD, providing exceptional value for comprehensive chromosomal analysis.

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Multiplex Fluorescence In Situ Hybridization (mFISH) Genetic Testing

Comprehensive Introduction to mFISH Testing

Multiplex Fluorescence In Situ Hybridization (mFISH) represents a revolutionary advancement in genetic diagnostics, offering unprecedented capabilities for chromosomal analysis. This sophisticated technique utilizes multiple fluorescent probes simultaneously to paint entire chromosomes with distinct colors, enabling comprehensive visualization of complex chromosomal rearrangements that traditional methods cannot detect. mFISH has transformed genetic testing by providing clinicians with detailed chromosomal maps essential for accurate diagnosis and personalized treatment strategies.

What mFISH Testing Measures and Detects

mFISH testing provides comprehensive analysis of chromosomal abnormalities through advanced fluorescent technology:

  • Complex Chromosomal Rearrangements: Identifies translocations, inversions, and complex rearrangements involving multiple chromosomes
  • Marker Chromosomes: Characterizes unknown chromosomal material and identifies their origins
  • Chromosomal Gains and Losses: Detects numerical abnormalities and structural variations
  • Cancer-Specific Abnormalities: Identifies chromosomal changes associated with hematological malignancies and solid tumors
  • Genetic Imbalances: Reveals unbalanced chromosomal rearrangements that may cause genetic disorders

Who Should Consider mFISH Testing

mFISH testing is recommended for individuals with specific clinical indications:

  • Cancer Patients: Individuals with hematological malignancies requiring comprehensive chromosomal analysis
  • Complex Genetic Cases: Patients with unexplained developmental delays or multiple congenital anomalies
  • Prenatal Screening: Cases with abnormal ultrasound findings or high-risk pregnancy indicators
  • Treatment Monitoring: Patients undergoing cancer treatment to monitor chromosomal response
  • Recurrent Miscarriages: Couples experiencing multiple pregnancy losses with unknown causes
  • Unexplained Infertility: Individuals with fertility issues where chromosomal factors are suspected

Significant Benefits of mFISH Testing

Choosing mFISH testing provides numerous advantages for comprehensive genetic assessment:

  • Comprehensive Analysis: Simultaneous evaluation of all 24 human chromosomes in a single test
  • High Resolution: Detection of complex rearrangements beyond conventional cytogenetic methods
  • Accurate Diagnosis: Precise identification of chromosomal abnormalities for targeted treatment
  • Prognostic Information: Valuable insights into disease progression and treatment response
  • Genetic Counseling Support: Essential information for family planning and genetic risk assessment
  • Treatment Guidance: Critical data for personalized medicine approaches and therapeutic decisions

Understanding Your mFISH Test Results

Interpreting mFISH results requires specialized expertise, but here’s general guidance:

  • Normal Results: Indicates no detectable chromosomal abnormalities in the analyzed sample
  • Specific Abnormalities: Identified chromosomal changes are detailed with precise breakpoints and involved chromosomes
  • Clinical Correlation: Results are interpreted in context with clinical symptoms and other diagnostic findings
  • Genetic Counseling: Abnormal results typically warrant consultation with genetic specialists
  • Treatment Implications: Specific chromosomal findings may guide targeted therapy selection
  • Follow-up Testing: Additional testing may be recommended based on initial mFISH findings

Test Pricing and Details

Test Component Details
Test Name Multiplex Fluorescence In Situ Hybridization (mFISH)
Discount Price $562 USD
Regular Price $750 USD
Turnaround Time 10-15 days
Sample Type Bone Marrow / Peripheral Blood
Test Components Sodium Heparin Vacutainer (2ml)
Prescription Required Doctor’s prescription required (not applicable for surgery, pregnancy, or travel abroad cases)

Nationwide Testing Availability

We proudly serve patients across the United States with comprehensive mFISH testing services. Our network includes testing facilities in all major metropolitan areas including New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, San Jose, and many other cities. No matter where you’re located in the USA, we can provide convenient access to advanced mFISH genetic testing.

Take Action for Your Genetic Health

Don’t wait to get the comprehensive chromosomal analysis you need. Our mFISH testing provides critical information for accurate diagnosis and personalized treatment planning. With our discounted price of $562 USD and nationwide availability, there’s no reason to delay this essential genetic assessment.

Call or WhatsApp us today at +1(267) 388-9828 to schedule your mFISH test appointment. Our genetic specialists are ready to answer your questions and help you understand how mFISH testing can benefit your specific situation. Take the first step toward comprehensive chromosomal analysis and personalized medical care.