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Ciliopathies Panel NGS Genetic DNA Test

Original price was: $750.Current price is: $500.

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The Ciliopathies Panel NGS Genetic DNA Test is a comprehensive diagnostic tool that utilizes next-generation sequencing technology to identify genetic mutations associated with ciliopathies – rare genetic disorders affecting cellular structures called cilia. This advanced test analyzes over 200 genes linked to conditions like Bardet-Biedl syndrome, Joubert syndrome, and primary ciliary dyskinesia. Priced at $500 USD, it provides crucial insights for patients experiencing developmental delays, vision problems, kidney dysfunction, or skeletal abnormalities. The test helps guide treatment decisions, enables early intervention, and provides valuable information for family planning. Results are typically available within 3-4 weeks from blood or DNA samples.

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  • ISO-Accredited Laboratory, Ensuring Highest Standards
  • Trusted by Hospitals & Patients —Accredited Testing with Results
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Ciliopathies Panel NGS Genetic DNA Test

Comprehensive Genetic Analysis for Ciliopathy Disorders

The Ciliopathies Panel NGS Genetic DNA Test represents a cutting-edge diagnostic approach for identifying genetic mutations associated with ciliopathies – a group of rare genetic disorders affecting cellular structures called cilia. These microscopic, hair-like projections play crucial roles in cellular signaling, fluid movement, and sensory perception throughout the body.

What Are Ciliopathies?

Ciliopathies are inherited conditions resulting from defects in cilia structure or function. These disorders can affect multiple organ systems including the eyes, kidneys, brain, skeletal system, and respiratory tract. Our comprehensive panel utilizes next-generation sequencing technology to provide accurate, reliable genetic analysis for patients and families affected by these complex conditions.

What the Test Measures and Detects

This advanced genetic panel analyzes over 200 genes associated with ciliopathy disorders, including:

  • Bardet-Biedl syndrome genes (BBS1, BBS2, BBS10, etc.)
  • Joubert syndrome-related genes (AHI1, CEP290, TMEM67)
  • Primary ciliary dyskinesia genes (DNAH5, DNAI1, CCDC40)
  • Skeletal dysplasia genes (COMP, COL10A1, TRPV4)
  • Nephronophthisis genes (NPHP1, NPHP3)
  • Meckel-Gruber syndrome genes (MKS1, TMEM216)
  • Oral-facial-digital syndrome genes (OFD1)

Who Should Consider This Test

Clinical Indications and Symptoms

This test is recommended for individuals presenting with:

  • Developmental delays or intellectual disability
  • Vision problems including retinal degeneration
  • Kidney dysfunction or polycystic kidney disease
  • Skeletal abnormalities or short stature
  • Respiratory issues including chronic sinusitis
  • Obesity with onset in childhood
  • Polydactyly (extra fingers or toes)
  • Hearing loss
  • Liver fibrosis
  • Family history of ciliopathy disorders

Benefits of Taking the Ciliopathies Panel Test

Comprehensive Diagnostic Advantages

  • Accurate Diagnosis: Provides definitive genetic confirmation of ciliopathy disorders
  • Early Intervention: Enables timely management and treatment planning
  • Family Planning: Offers crucial information for genetic counseling and reproductive decisions
  • Personalized Care: Guides targeted therapeutic approaches based on specific genetic findings
  • Prognostic Information: Helps predict disease progression and potential complications
  • Research Contribution: Advances understanding of rare genetic disorders

Understanding Your Test Results

Interpreting Genetic Findings

Your test results will be carefully analyzed and interpreted by our team of genetic specialists. Results typically fall into three categories:

Positive Result

A positive result indicates the presence of pathogenic mutations associated with ciliopathy disorders. This confirmation enables:

  • Targeted medical management
  • Specialist referrals as needed
  • Family member testing recommendations
  • Long-term monitoring plans

Negative Result

A negative result suggests that no known pathogenic mutations were detected in the genes analyzed. However, this doesn’t completely rule out a genetic condition, as new genes continue to be discovered.

Variant of Uncertain Significance (VUS)

Some genetic changes may be classified as VUS, meaning their clinical significance is currently unknown. Our genetic counselors will provide guidance on monitoring and potential follow-up testing.

Test Information and Pricing

Test Parameter Details
Test Name Ciliopathies Panel NGS Genetic DNA Test
Discount Price $500 USD
Regular Price $750 USD
Turnaround Time 3 to 4 Weeks
Sample Type Blood, Extracted DNA, or One Drop Blood on FTA Card
Methodology Next-Generation Sequencing (NGS) Technology
Specialty Pediatrics, Genetics

Nationwide Availability and Booking

We have diagnostic centers conveniently located across the United States, serving patients in all major metropolitan areas including New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, and San Jose. Our state-of-the-art facilities ensure consistent, high-quality testing standards nationwide.

Ready to Schedule Your Test?

Take the first step toward accurate diagnosis and personalized care. Our genetic counseling team is available to discuss your testing options and answer any questions you may have.

Call or WhatsApp us today at +1(267) 388-9828 to book your Ciliopathies Panel NGS Genetic DNA Test.

Early genetic testing can provide crucial insights for managing ciliopathy disorders and improving quality of life. Don’t wait – schedule your comprehensive genetic evaluation today.