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FGF23 Gene Hypophosphatemic Rickets Autosomal Dominant Genetic Test

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

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The FGF23 Gene Hypophosphatemic Rickets Autosomal Dominant NGS Genetic DNA Test is a cutting-edge genetic analysis that identifies mutations in the FGF23 gene responsible for hereditary hypophosphatemic rickets. This comprehensive test utilizes Next-Generation Sequencing (NGS) technology to detect autosomal dominant inheritance patterns of this metabolic bone disorder. The test is crucial for individuals experiencing symptoms like bone pain, skeletal deformities, growth retardation, and dental abnormalities. Early detection through this $500 USD test enables proactive management strategies, prevents long-term complications, and provides valuable information for family planning decisions. Our advanced genetic testing helps healthcare providers develop personalized treatment plans and monitor disease progression effectively.

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FGF23 Gene Hypophosphatemic Rickets Autosomal Dominant NGS Genetic DNA Test

Comprehensive Genetic Testing for Hereditary Bone Metabolism Disorders

The FGF23 Gene Hypophosphatemic Rickets Autosomal Dominant NGS Genetic DNA Test represents a breakthrough in genetic diagnostics for hereditary bone metabolism disorders. This advanced test specifically targets mutations in the Fibroblast Growth Factor 23 (FGF23) gene, which plays a critical role in phosphate regulation and bone mineralization. Utilizing cutting-edge Next-Generation Sequencing technology, our test provides unparalleled accuracy in detecting autosomal dominant inheritance patterns of hypophosphatemic rickets, enabling early intervention and personalized treatment strategies.

What Does This Test Measure and Detect?

This comprehensive genetic analysis specifically identifies:

  • Pathogenic variants in the FGF23 gene responsible for autosomal dominant hypophosphatemic rickets
  • Single nucleotide polymorphisms (SNPs) affecting phosphate metabolism
  • Genetic mutations that disrupt normal bone mineralization processes
  • Inheritance patterns to determine familial risk assessment
  • Specific genetic markers associated with treatment response

Who Should Consider This Genetic Test?

This test is recommended for individuals experiencing:

  • Unexplained bone pain and skeletal deformities
  • Growth retardation or short stature in childhood
  • Dental abnormalities including enamel defects and abscesses
  • Family history of hypophosphatemic rickets or bone disorders
  • Persistent low phosphate levels in blood tests
  • Bowing of legs or other skeletal abnormalities
  • Muscle weakness and fatigue unrelated to other causes

Key Benefits of FGF23 Genetic Testing

Early genetic diagnosis through our comprehensive testing provides numerous advantages:

  • Early Intervention: Enables proactive treatment before severe complications develop
  • Personalized Treatment: Guides healthcare providers in developing targeted therapy plans
  • Family Planning: Provides crucial information for genetic counseling and reproductive decisions
  • Prevention of Complications: Helps prevent bone deformities, growth issues, and dental problems
  • Accurate Diagnosis: Differentiates between various types of rickets and bone disorders
  • Monitoring Progression: Establishes baseline for ongoing disease management

Understanding Your Test Results

Our comprehensive genetic report provides clear, actionable information:

  • Positive Result: Indicates presence of FGF23 gene mutation; consult with genetic specialist for management plan
  • Negative Result: Suggests absence of tested mutations; other causes for symptoms should be investigated
  • Variant of Uncertain Significance: Requires additional clinical correlation and possibly family testing
  • Carrier Status: Important information for family members and future generations

All results include detailed interpretation by our board-certified genetic specialists, with recommendations for next steps and appropriate referrals.

Test Pricing and Details

Test Component Details
Test Name FGF23 Gene Hypophosphatemic Rickets Autosomal Dominant 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

Pre-Test Requirements

To ensure accurate results and comprehensive care, we require:

  • Complete clinical history of the patient
  • Genetic counseling session to create detailed family pedigree
  • Documentation of affected family members with hypophosphatemic rickets
  • Current symptoms and previous diagnostic test results

Nationwide Accessibility

We have diagnostic centers conveniently located across the United States, serving major metropolitan areas including New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, and many other cities. Our network ensures accessible genetic testing services for patients nationwide.

Take Control of Your Genetic Health Today

Don’t let uncertainty about hereditary bone disorders affect your quality of life. Our FGF23 Gene Hypophosphatemic Rickets Autosomal Dominant NGS Genetic DNA Test provides the clarity you need for informed healthcare decisions. With our special discounted price of $500 USD, advanced genetic testing is more accessible than ever.

Call or WhatsApp us today at +1(267) 388-9828 to schedule your genetic counseling session and book your test. Our genetic specialists are ready to guide you through the testing process and help you understand your results.

Early detection through comprehensive genetic testing can make a significant difference in managing hereditary bone disorders and preventing long-term complications. Trust our expertise in metabolic genetics to provide you with accurate, reliable results and personalized care.