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FLNB Gene Atelosteogenesis Type 3 Genetic Test

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

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The FLNB Gene Atelosteogenesis Type 3 NGS Genetic DNA Test is a comprehensive genetic analysis that identifies mutations in the FLNB gene responsible for Atelosteogenesis Type 3, a rare skeletal dysplasia disorder. Using advanced Next-Generation Sequencing (NGS) technology, this test provides precise detection of genetic variants that affect bone development and skeletal formation. The test is crucial for individuals showing symptoms of skeletal abnormalities, joint dislocations, or family history of bone disorders. Results help guide treatment decisions, provide genetic counseling insights, and enable early intervention strategies. This specialized test costs $500 USD and offers valuable information for managing skeletal health and genetic inheritance patterns.

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FLNB Gene Atelosteogenesis Type 3 NGS Genetic DNA Test

Comprehensive Genetic Analysis for Skeletal Disorders

The FLNB Gene Atelosteogenesis Type 3 NGS Genetic DNA Test represents a breakthrough in genetic diagnostics for skeletal dysplasia conditions. This advanced test utilizes cutting-edge Next-Generation Sequencing technology to analyze the FLNB gene, which plays a critical role in skeletal development and bone formation. Atelosteogenesis Type 3 is a rare genetic disorder characterized by abnormal bone growth and development, and early detection through genetic testing can significantly impact treatment outcomes and quality of life.

What Does This Test Measure and Detect?

This comprehensive genetic test specifically targets the FLNB (Filamin B) gene, which encodes a protein essential for proper skeletal development and joint formation. The test detects:

  • Pathogenic mutations in the FLNB gene associated with Atelosteogenesis Type 3
  • Genetic variants affecting bone growth and development
  • Mutations responsible for skeletal dysplasia and joint abnormalities
  • Inheritance patterns for genetic counseling purposes
  • Specific genetic markers that influence treatment approaches

Who Should Consider This Test?

Clinical Indications and Symptoms

This test is recommended for individuals presenting with the following symptoms or clinical scenarios:

  • Newborns or children with skeletal abnormalities and joint dislocations
  • Individuals with family history of skeletal dysplasia disorders
  • Patients showing signs of abnormal bone growth and development
  • Those with unexplained joint laxity or skeletal malformations
  • Families seeking genetic counseling for skeletal disorder inheritance
  • Individuals with suspected FLNB-related disorders based on clinical evaluation

Benefits of Taking the FLNB Genetic Test

Undergoing this comprehensive genetic analysis provides numerous advantages for patients and healthcare providers:

  • Accurate Diagnosis: Provides definitive genetic confirmation of Atelosteogenesis Type 3
  • Personalized Treatment: Enables targeted treatment strategies based on genetic findings
  • Genetic Counseling: Supports informed family planning decisions
  • Early Intervention: Facilitates early management of skeletal complications
  • Comprehensive Analysis: Utilizes advanced NGS technology for thorough genetic assessment
  • Clinical Guidance: Helps healthcare providers develop appropriate care plans

Understanding Your Test Results

Your FLNB Gene Atelosteogenesis Type 3 NGS Genetic DNA Test results will provide comprehensive information about your genetic status:

  • Positive Result: Indicates the presence of FLNB gene mutations associated with Atelosteogenesis Type 3, requiring specialized medical management
  • Negative Result: Suggests no detected FLNB mutations, though clinical correlation with symptoms is essential
  • Variant of Uncertain Significance: Identifies genetic changes whose clinical significance requires further evaluation
  • Carrier Status: Determines if you carry FLNB mutations that could be passed to offspring

All results are accompanied by detailed interpretation and recommendations from our genetic specialists. We recommend discussing your results with a qualified genetic counselor or healthcare provider to fully understand the implications for your health and family planning.

Test Pricing and Details

Test Component Price (USD)
Discount Price $500
Regular Price $700
Turnaround Time 3 to 4 Weeks
Sample Type Blood, Extracted DNA, or One Drop Blood on FTA Card

Pre-Test Requirements

Before undergoing the FLNB Gene Atelosteogenesis Type 3 NGS Genetic DNA Test, patients should provide:

  • Complete clinical history of the patient
  • Genetic counseling session to create a detailed family pedigree chart
  • Documentation of family members affected by skeletal disorders
  • Relevant medical records and previous test results

Nationwide Testing Availability

We have testing facilities and collection centers across the United States, including major metropolitan areas such as New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, San Jose, and many other cities. Our nationwide network ensures convenient access to advanced genetic testing services regardless of your location.

Take Control of Your Genetic Health Today

Don’t let uncertainty about skeletal disorders affect your quality of life. The FLNB Gene Atelosteogenesis Type 3 NGS Genetic DNA Test provides the clarity and information needed to make informed healthcare decisions. Our team of genetic specialists and healthcare professionals is ready to support you through every step of the testing process.

Call or WhatsApp us today at +1(267) 388-9828 to schedule your genetic test consultation and take the first step toward understanding your genetic health.

Our comprehensive genetic testing services combine advanced technology with expert interpretation to deliver reliable results you can trust. Book your FLNB Gene Atelosteogenesis Type 3 NGS Genetic DNA Test now and gain valuable insights into your skeletal health and genetic inheritance patterns.