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FKBP10 Gene Osteogenesis Imperfecta Type 11 NGS Genetic DNA Test

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

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The FKBP10 Gene Osteogenesis Imperfecta Type 11 NGS Genetic DNA Test is a cutting-edge genetic analysis that identifies mutations in the FKBP10 gene responsible for Osteogenesis Imperfecta Type 11. This comprehensive test utilizes Next-Generation Sequencing (NGS) technology to detect specific genetic variations that cause brittle bone disease, collagen formation disorders, and skeletal abnormalities. The test is crucial for individuals experiencing recurrent fractures, bone deformities, or family history of bone disorders. Results provide definitive diagnosis, enable personalized treatment planning, and offer valuable insights for family genetic counseling. Available for only $500 USD, this advanced genetic test delivers critical information for managing bone health and preventing complications.

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FKBP10 Gene Osteogenesis Imperfecta Type 11 NGS Genetic DNA Test

Comprehensive Genetic Analysis for Bone Health

The FKBP10 Gene Osteogenesis Imperfecta Type 11 NGS Genetic DNA Test represents a breakthrough in genetic diagnostics for bone disorders. This advanced Next-Generation Sequencing (NGS) test specifically targets the FKBP10 gene, which plays a critical role in collagen processing and bone matrix formation. Osteogenesis Imperfecta Type 11 is a rare genetic condition characterized by bone fragility, skeletal deformities, and increased fracture risk. Understanding your genetic predisposition through this test can transform your approach to bone health management and treatment planning.

What Does This Test Measure?

This comprehensive genetic test utilizes state-of-the-art NGS technology to analyze the entire FKBP10 gene sequence, detecting:

  • Point mutations and single nucleotide variations
  • Insertions and deletions affecting gene function
  • Missense, nonsense, and frameshift mutations
  • Regulatory region variations impacting gene expression
  • Compound heterozygous mutations

The test specifically examines mutations that disrupt the FKBP65 protein function, essential for proper collagen triple-helix formation and bone mineralization processes.

Who Should Consider This Genetic Test?

Clinical Indications and Symptoms

This test is recommended for individuals presenting with:

  • Recurrent fractures with minimal trauma
  • Family history of Osteogenesis Imperfecta
  • Blue sclerae (white part of eyes)
  • Dentinogenesis imperfecta (tooth abnormalities)
  • Progressive bone deformities
  • Short stature with bone fragility
  • Hearing loss in childhood or adolescence
  • Joint hypermobility with bone weakness
  • Abnormal bone density measurements
  • Suspected collagen formation disorders

Key Benefits of Genetic Testing

Undergoing the FKBP10 genetic test provides numerous advantages:

  • Definitive Diagnosis: Confirm or rule out Osteogenesis Imperfecta Type 11 with precision
  • Personalized Treatment: Develop targeted therapeutic strategies based on genetic findings
  • Family Planning: Understand inheritance patterns and recurrence risks
  • Early Intervention: Implement preventive measures before severe complications develop
  • Comprehensive Care: Coordinate multidisciplinary management involving orthopedics, genetics, and rehabilitation
  • Psychological Relief: Reduce uncertainty and provide clear answers about your condition

Understanding Your Test Results

Interpretation Guidelines

Your genetic test results will fall into one of these categories:

  • Positive Result: Identified pathogenic mutation confirms Osteogenesis Imperfecta Type 11 diagnosis, enabling targeted management and family screening
  • Negative Result: No FKBP10 mutations detected, suggesting alternative causes for symptoms requiring further investigation
  • Variant of Uncertain Significance: Genetic changes with unclear clinical impact, necessitating periodic re-evaluation as research advances
  • Carrier Status: Identification of individuals with one mutated copy who may pass the condition to offspring

All results include comprehensive genetic counseling to ensure proper understanding and appropriate next steps.

Test Pricing and Details

Test Component Details
Test Name FKBP10 Gene Osteogenesis Imperfecta Type 11 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

Before scheduling your test, please ensure:

  • Complete clinical history documentation
  • Genetic counseling session to create family pedigree chart
  • Discussion of testing implications with healthcare provider
  • Understanding of potential outcomes and their significance

Nationwide Testing Availability

We proudly serve patients across the United States with convenient testing locations in all major cities including New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, and San Jose. Our state-of-the-art genetic testing facilities ensure consistent, reliable results regardless of your location.

Take Control of Your Bone Health Today

Don’t let uncertainty about your bone health condition affect your quality of life. The FKBP10 Gene Osteogenesis Imperfecta Type 11 NGS Genetic DNA Test provides the clarity you need for informed medical decisions and comprehensive care planning. Our expert genetic counselors and medical professionals are ready to guide you through every step of the testing process.

Ready to begin your genetic testing journey? Contact us today to schedule your appointment or speak with our genetic counseling team.

Call or WhatsApp: +1(267) 388-9828

Book your FKBP10 genetic test now and take the first step toward understanding your bone health at the genetic level. Our dedicated team is committed to providing accurate results, comprehensive support, and personalized guidance throughout your testing experience.