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Haemophilia A & B Gene Panel

Original price was: $1,200.Current price is: $900.

-25%

The Haemophilia A & B Gene Panel is a comprehensive genetic test that analyzes mutations in the F8 and F8 genes responsible for haemophilia A and B. This advanced diagnostic tool uses Next-Generation Sequencing (NGS) technology to identify specific genetic variations that cause these inherited bleeding disorders. The test is crucial for individuals with unexplained bleeding tendencies, family history of haemophilia, or those planning pregnancy. Results provide valuable information for personalized treatment strategies, genetic counseling, and family planning decisions. The test requires a peripheral blood sample and has a turnaround time of 4-6 weeks. Available for $900 USD, this panel offers significant savings from the regular $1200 USD price.

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Haemophilia A & B Gene Panel

Comprehensive Genetic Testing for Inherited Bleeding Disorders

The Haemophilia A & B Gene Panel represents a cutting-edge diagnostic approach to identifying genetic mutations responsible for haemophilia, a group of inherited bleeding disorders affecting approximately 1 in 5,000 males worldwide. This comprehensive genetic analysis provides crucial insights into the underlying causes of abnormal bleeding tendencies, enabling precise diagnosis and personalized treatment strategies.

What Does the Haemophilia A & B Gene Panel Measure?

This advanced genetic panel utilizes Next-Generation Sequencing (NGS) technology to thoroughly examine two critical genes:

  • F8 Gene Analysis: Comprehensive screening for mutations in the Factor VIII gene located on the X chromosome, responsible for haemophilia A
  • F9 Gene Analysis: Detailed examination of the Factor IX gene mutations that cause haemophilia B
  • Variant Detection: Identifies point mutations, deletions, insertions, and other genetic variations affecting clotting factor production
  • Carrier Status: Determines carrier status in females who may pass the condition to their children

Who Should Consider This Genetic Test?

This comprehensive genetic panel is recommended for individuals experiencing:

  • Unexplained or excessive bleeding following minor injuries or surgeries
  • Frequent nosebleeds without apparent cause
  • Easy bruising or large bruises from minor trauma
  • Joint pain and swelling due to internal bleeding
  • Family history of haemophilia or bleeding disorders
  • Women with family history planning pregnancy
  • Individuals with abnormal coagulation test results
  • Those requiring definitive diagnosis for treatment planning

Key Benefits of Haemophilia Genetic Testing

  • Accurate Diagnosis: Provides definitive identification of specific genetic mutations
  • Personalized Treatment: Enables tailored treatment plans based on genetic profile
  • Family Planning Guidance: Offers valuable information for genetic counseling and reproductive decisions
  • Early Intervention: Facilitates proactive management before serious bleeding complications occur
  • Carrier Detection: Identifies female carriers who may pass the condition to offspring
  • Treatment Monitoring: Helps track treatment effectiveness and adjust therapies as needed

Understanding Your Test Results

Your Haemophilia A & B Gene Panel results will provide detailed information about your genetic status:

  • Positive Result: Indicates the presence of a known disease-causing mutation in either F8 or F9 gene
  • Negative Result: Suggests no detectable mutations associated with haemophilia A or B
  • Carrier Status: For females, identifies whether you carry one copy of a mutated gene
  • Variant of Unknown Significance: May identify genetic changes with unclear clinical implications requiring further evaluation

All results are accompanied by comprehensive interpretation from our genetic specialists, who will explain the implications for your health and provide guidance on next steps.

Test Details and Pricing

Test Component Details
Test Name Haemophilia A & B Gene Panel
Discount Price $900 USD
Regular Price $1200 USD
Turnaround Time 4-6 weeks
Sample Type Peripheral Blood
Test Components EDTA Vacutainer (3 ml)
Testing Method Next-Generation Sequencing (NGS)

Pre-Test Instructions

The Haemophilia A & B Gene Panel requires a doctor’s prescription for testing. Please note that prescriptions are not applicable for surgery and pregnancy cases or individuals planning to travel abroad. Our team will guide you through the sample collection process and ensure proper handling of your genetic material.

Nationwide Testing Availability

We have convenient testing locations across the United States, including major cities such as New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, San Jose, and many more. Our network of certified collection centers ensures accessible testing regardless of your location.

Take Control of Your Genetic Health Today

Don’t let uncertainty about bleeding disorders affect your quality of life. The Haemophilia A & B Gene Panel provides the clarity you need for informed healthcare decisions. Our genetic specialists are available to discuss your results and provide comprehensive guidance.

Book your Haemophilia A & B Gene Panel 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 proper management of potential bleeding disorders.