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Dysmorphology Panel NGS Genetic DNA Test

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

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The Dysmorphology Panel NGS Genetic DNA Test is a comprehensive genetic analysis designed to identify underlying genetic causes of congenital anomalies and dysmorphic features. Using advanced Next Generation Sequencing technology, this panel examines over 500 genes associated with various dysmorphology syndromes, birth defects, and developmental abnormalities. This test provides crucial diagnostic information for children and adults presenting with unexplained physical anomalies, helping clinicians establish accurate diagnoses and develop targeted management strategies. The test costs $500 USD and is particularly valuable for pediatric patients with complex presentations. Results are typically available within 3-4 weeks, providing families with timely genetic insights for informed medical decision-making.

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Dysmorphology Panel NGS Genetic DNA Test

Comprehensive Genetic Analysis for Congenital Anomalies

The Dysmorphology Panel NGS Genetic DNA Test represents a cutting-edge diagnostic approach for identifying genetic causes of congenital anomalies and dysmorphic features. This comprehensive genetic panel utilizes Next Generation Sequencing (NGS) technology to analyze over 500 genes associated with various dysmorphology syndromes, providing clinicians with powerful diagnostic insights for patients presenting with complex physical abnormalities.

What This Advanced Genetic Test Measures

Our comprehensive dysmorphology panel detects genetic variants across multiple gene categories including:

  • Skeletal Dysplasia Genes: COL1A1, COL1A2, COL2A1, and other collagen-related genes
  • Craniofacial Anomaly Genes: FGFR1, FGFR2, FGFR3, TWIST1, and related pathways
  • Neurological Development Genes: TUBB, TUBA1A, DYNC1H1, and microtubule-associated genes
  • Metabolic Disorder Genes: EBP, DHCR7, and cholesterol biosynthesis pathways
  • Cardiac Development Genes: NKX2-5, TBX5, and heart formation regulators
  • Ciliopathy Genes: BBS1, BBS10, CEP290, and ciliary function genes

Who Should Consider This Genetic Test?

This comprehensive panel is particularly valuable for individuals presenting with:

  • Unexplained congenital anomalies or multiple birth defects
  • Dysmorphic facial features without established diagnosis
  • Skeletal abnormalities including short stature or limb anomalies
  • Neurological abnormalities with associated physical features
  • Family history of similar congenital conditions
  • Complex medical presentations involving multiple organ systems
  • Developmental delays with accompanying physical anomalies

Clinical Benefits of Dysmorphology Genetic Testing

Undergoing comprehensive genetic testing provides numerous clinical advantages:

  • Accurate Diagnosis: Establish definitive genetic diagnoses for complex presentations
  • Personalized Management: Develop targeted treatment and monitoring strategies
  • Family Planning: Provide recurrence risk information for future pregnancies
  • Prognostic Information: Understand potential disease progression and outcomes
  • Medical Intervention: Guide surgical planning and medical management
  • Early Intervention: Enable timely therapeutic interventions when available

Understanding Your Genetic Test Results

Our comprehensive genetic analysis provides detailed insights into your genetic profile:

  • Pathogenic Variants: Clearly identified disease-causing mutations with clinical significance
  • Likely Pathogenic Variants: Strongly suspected disease-associated variants requiring confirmation
  • Variants of Uncertain Significance: Genetic changes requiring additional clinical correlation
  • Benign Variants: Common genetic variations without clinical implications
  • Carrier Status: Information about recessive conditions that may affect future generations

All results are accompanied by detailed interpretation from our board-certified genetic counselors and clinical geneticists, ensuring you receive comprehensive guidance for understanding and acting upon your genetic information.

Test Pricing and Availability

Test Component Price (USD)
Dysmorphology Panel NGS Genetic DNA Test – Discount Price $500
Dysmorphology Panel NGS Genetic DNA Test – Regular Price $750
Turnaround Time 3-4 Weeks
Sample Type Blood, Extracted DNA, or One Drop Blood on FTA Card

Nationwide Testing Availability

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, Austin, Jacksonville, Fort Worth, Columbus, Charlotte, San Francisco, Indianapolis, Seattle, Denver, Washington DC, Boston, El Paso, Nashville, Detroit, Oklahoma City, Portland, Las Vegas, Memphis, Louisville, Baltimore, Milwaukee, Albuquerque, Tucson, Fresno, Sacramento, Mesa, Kansas City, Atlanta, Colorado Springs, Omaha, Raleigh, Miami, Long Beach, Virginia Beach, Oakland, Minneapolis, Tulsa, Arlington, and Tampa.

Take the Next Step Toward Genetic Clarity

If you or your child presents with unexplained congenital anomalies or dysmorphic features, our comprehensive genetic testing can provide the answers you need. Our experienced genetic counselors are available to discuss your specific situation and determine if this advanced testing is appropriate for your needs.

Call us today at +1(267) 388-9828 to schedule your genetic counseling session and book your Dysmorphology Panel NGS Genetic DNA Test. Our team is committed to providing you with comprehensive genetic insights and personalized support throughout your diagnostic journey.