Sale!

B3GALT6 Gene Spondyloepimetaphyseal Dysplasia with Joint Laxity Type 1 NGS Genetic DNA Test

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

-29%

The B3GALT6 Gene Spondyloepimetaphyseal Dysplasia with Joint Laxity Type 1 NGS Genetic DNA Test is a comprehensive diagnostic tool that identifies mutations in the B3GALT6 gene responsible for a rare connective tissue disorder. This advanced next-generation sequencing test detects genetic variations causing skeletal abnormalities, joint hypermobility, skin elasticity issues, and increased fracture risk. The test provides crucial information for accurate diagnosis, enabling personalized treatment strategies and genetic counseling. Available for $500 USD, this specialized genetic analysis helps patients and families understand their condition and make informed healthcare decisions. Results are typically available within 3-4 weeks from sample collection.

Clinically Validated & Lab Certified

  • ISO-Accredited Laboratory, Ensuring Highest Standards
  • Trusted by Hospitals & Patients —Accredited Testing with Results
  • Direct Healthcare Provider Support + Comprehensive Reporting
Guaranteed Safe Checkout

B3GALT6 Gene Spondyloepimetaphyseal Dysplasia with Joint Laxity Type 1 NGS Genetic DNA Test

Comprehensive Genetic Testing for Rare Connective Tissue Disorders

The B3GALT6 Gene Spondyloepimetaphyseal Dysplasia with Joint Laxity Type 1 NGS Genetic DNA Test represents a breakthrough in genetic diagnostics for rare skeletal and connective tissue disorders. This specialized test utilizes cutting-edge Next-Generation Sequencing (NGS) technology to identify mutations in the B3GALT6 gene, which plays a critical role in proteoglycan synthesis and connective tissue integrity.

What This Test Measures and Detects

Our advanced NGS genetic test specifically targets the B3GALT6 gene to identify pathogenic variants associated with:

  • Mutations causing spondyloepimetaphyseal dysplasia with joint laxity type 1
  • Genetic variations affecting proteoglycan biosynthesis
  • Inherited patterns of connective tissue abnormalities
  • Specific nucleotide changes impacting skeletal development
  • Variants associated with increased fracture susceptibility

Who Should Consider This Genetic Test

This comprehensive genetic analysis is recommended for individuals presenting with:

  • Unexplained joint hypermobility and recurrent dislocations
  • Progressive skeletal abnormalities and short stature
  • History of multiple fractures with minimal trauma
  • Family history of connective tissue disorders
  • Characteristic facial features associated with SEMDJL1
  • Skin hyperelasticity and abnormal scarring
  • Developmental delays with skeletal involvement
  • Suspected inherited skeletal dysplasia conditions

Clinical Benefits of Genetic Testing

Undergoing the B3GALT6 genetic test provides numerous advantages for patients and healthcare providers:

  • Accurate Diagnosis: Confirms or rules out SEMDJL1 with precision
  • Personalized Treatment: Enables targeted management strategies
  • Genetic Counseling: Provides family planning guidance
  • Early Intervention: Facilitates proactive care planning
  • Comprehensive Understanding: Clarifies disease progression and prognosis
  • Research Contribution: Advances medical knowledge of rare disorders

Understanding Your Test Results

Our genetic specialists provide comprehensive interpretation of your results:

  • Positive Result: Identifies a pathogenic variant in the B3GALT6 gene, confirming SEMDJL1 diagnosis
  • Negative Result: No disease-causing mutations detected in the B3GALT6 gene
  • Variant of Uncertain Significance: Identifies genetic changes with unknown clinical impact requiring further evaluation
  • Carrier Status: Determines if you carry one copy of a mutated gene

All results include detailed explanations and recommendations for next steps, including consultation with genetic specialists and appropriate medical management.

Test Specifications and Pricing

Test Component Details
Test Name B3GALT6 Gene Spondyloepimetaphyseal Dysplasia with Joint Laxity Type 1 NGS Genetic DNA Test
Regular Price $700 USD
Discount Price $500 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 Accessibility

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, San Jose, and many more. Our network of certified genetic testing facilities ensures accessible, reliable service nationwide.

Take the Next Step Toward Genetic Clarity

Don’t let uncertainty about your genetic health hold you back. Our specialized B3GALT6 genetic test provides the answers you need for informed medical decisions and personalized care planning. With our discounted price of $500 USD and comprehensive genetic analysis, you can gain valuable insights into your connective tissue health.

Ready to schedule your genetic test? Contact our genetic specialists today at +1(267) 388-9828 or book your appointment online. Take control of your genetic health journey with confidence and clarity.