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CCDC28B Gene Bardet-Biedl Syndrome Modifier NGS Genetic DNA Test

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

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The CCDC28B Gene Bardet-Biedl Syndrome Modifier NGS Genetic DNA Test is a comprehensive genetic analysis that identifies mutations in the CCDC28B gene, which acts as a modifier in Bardet-Biedl syndrome. This advanced next-generation sequencing test provides crucial information for patients experiencing symptoms affecting multiple organ systems including vision, kidney function, endocrine regulation, and development. For $500 USD, this test offers precise genetic diagnosis, enabling personalized treatment strategies and family planning decisions. The test requires a simple blood sample or extracted DNA and provides results within 3-4 weeks, making it an essential tool for individuals with suspected genetic disorders involving hepatology, nephrology, and endocrinology systems.

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CCDC28B Gene Bardet-Biedl Syndrome Modifier NGS Genetic DNA Test

Comprehensive Genetic Analysis for Complex Disorders

The CCDC28B Gene Bardet-Biedl Syndrome Modifier NGS Genetic DNA Test represents a cutting-edge approach to diagnosing complex genetic conditions that affect multiple organ systems. This specialized test focuses on the CCDC28B gene, which plays a crucial role as a modifier in Bardet-Biedl syndrome – a rare genetic disorder characterized by progressive vision loss, kidney abnormalities, obesity, and developmental challenges.

What This Advanced Genetic Test Measures

Our NGS (Next-Generation Sequencing) technology provides comprehensive analysis of the CCDC28B gene to detect:

  • Point mutations and single nucleotide variants
  • Small insertions and deletions
  • Copy number variations
  • Complex genetic rearrangements
  • Modifier effects on Bardet-Biedl syndrome presentation

Who Should Consider This Genetic Test?

This test is particularly recommended for individuals experiencing symptoms across multiple organ systems, including:

Vision-Related Symptoms

  • Progressive vision loss beginning in childhood
  • Retinal dystrophy or rod-cone dystrophy
  • Night blindness and photophobia
  • Visual field constriction

Renal and Hepatic Concerns

  • Kidney abnormalities or renal dysfunction
  • Hepatic involvement or liver complications
  • Structural kidney malformations
  • Progressive renal failure

Endocrine and Developmental Issues

  • Early-onset obesity
  • Growth abnormalities
  • Hormonal imbalances
  • Developmental delays
  • Learning disabilities

Significant Benefits of Genetic Testing

Undergoing the CCDC28B genetic test provides numerous advantages for patients and families:

Accurate Diagnosis and Prognosis

Receive definitive genetic confirmation of Bardet-Biedl syndrome and understand how CCDC28B modifications affect disease severity and progression.

Personalized Treatment Planning

Genetic results enable healthcare providers to develop targeted management strategies for vision, kidney, endocrine, and developmental concerns.

Family Planning Guidance

Understand inheritance patterns and recurrence risks for future pregnancies, empowering informed reproductive decisions.

Early Intervention Opportunities

Identify at-risk family members before symptom onset, allowing for proactive monitoring and preventive care.

Understanding Your Test Results

Our comprehensive genetic counseling support helps you interpret your results:

Positive Results

A positive result indicates the presence of CCDC28B gene mutations that modify Bardet-Biedl syndrome expression. This information guides specialized care coordination across multiple medical specialties.

Negative Results

A negative result suggests that CCDC28B mutations are not contributing to your symptoms, allowing physicians to explore alternative diagnostic possibilities.

Variant of Uncertain Significance

Some genetic changes may require additional family studies or research correlation to determine clinical significance.

Test Details and Pricing

Test Component Details Price (USD)
Test Name CCDC28B Gene Bardet-Biedl Syndrome Modifier NGS Genetic DNA Test
Discount Price Limited Time Offer $500
Regular Price Standard Rate $700
Turnaround Time Comprehensive Analysis 3-4 Weeks
Sample Type Multiple Options Available Blood, Extracted DNA, or FTA Card

Nationwide Accessibility

We proudly serve patients across the United States with convenient testing locations in all major metropolitan areas including New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, San Jose, and many more cities. Our network of certified genetic counselors and healthcare professionals ensures you receive comprehensive support regardless of your location.

Take the Next Step Toward Genetic Clarity

Don’t let uncertainty about your genetic health prevent you from getting the answers you need. Our team of genetic specialists is ready to guide you through the testing process and help you understand your results.

Call or WhatsApp us today at +1(267) 388-9828 to schedule your genetic counseling session and book your CCDC28B genetic test. Take control of your health journey with definitive genetic information that can transform your medical care and quality of life.

Pre-Test Requirements

Before your test, please provide:

  • Complete clinical history relevant to Bardet-Biedl syndrome symptoms
  • Participation in genetic counseling to create a detailed family pedigree
  • Information about affected family members and their symptoms

Our genetic counseling team will help you prepare all necessary documentation and ensure you’re fully informed about the testing process and potential outcomes.