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FGFR2 Gene LADD Syndrome NGS Genetic DNA Test

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

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The FGFR2 Gene LADD Syndrome NGS Genetic DNA Test is a comprehensive genetic analysis that detects mutations in the FGFR2 gene associated with Lacrimo-Auriculo-Dento-Digital (LADD) syndrome. This advanced next-generation sequencing test provides crucial diagnostic information for individuals presenting with characteristic craniofacial abnormalities, limb malformations, and developmental concerns. The test helps confirm clinical diagnoses, guide treatment strategies, and provide valuable information for family planning. Available for only $500 USD, this specialized genetic testing offers precise identification of pathogenic variants responsible for this rare congenital disorder affecting multiple body systems including facial features, tear ducts, ears, teeth, and fingers.

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FGFR2 Gene LADD Syndrome NGS Genetic DNA Test

Comprehensive Genetic Analysis for LADD Syndrome

The FGFR2 Gene LADD Syndrome NGS Genetic DNA Test represents a cutting-edge diagnostic tool designed to identify mutations in the fibroblast growth factor receptor 2 (FGFR2) gene associated with Lacrimo-Auriculo-Dento-Digital (LADD) syndrome. This rare genetic disorder affects multiple body systems, primarily involving craniofacial development, limb formation, and various organ systems. Our advanced next-generation sequencing technology provides unparalleled accuracy in detecting pathogenic variants that contribute to this complex congenital condition.

What Does This Test Measure and Detect?

This comprehensive genetic test specifically targets the FGFR2 gene, which plays a critical role in embryonic development, particularly in bone growth and tissue formation. The test identifies:

  • Pathogenic mutations in the FGFR2 gene associated with LADD syndrome
  • Single nucleotide variants (SNVs) and small insertions/deletions (indels)
  • Copy number variations (CNVs) affecting the FGFR2 gene region
  • Novel genetic variants with potential clinical significance
  • Inheritance patterns that may impact family members

Who Should Consider This Test?

This genetic test is recommended for individuals presenting with characteristic symptoms of LADD syndrome, including:

  • Newborns and children with craniofacial abnormalities
  • Individuals with lacrimal duct abnormalities or excessive tearing
  • Patients with ear malformations or hearing difficulties
  • Those with dental anomalies including missing or malformed teeth
  • Individuals with digital abnormalities such as syndactyly or clinodactyly
  • Patients with a family history of LADD syndrome or related craniofacial disorders
  • Individuals with unexplained developmental delays affecting multiple systems

Clinical Benefits of Genetic Testing

Undergoing the FGFR2 Gene LADD Syndrome NGS Genetic DNA Test provides numerous clinical advantages:

  • Accurate Diagnosis: Confirms or rules out LADD syndrome with high precision
  • Personalized Treatment Planning: Guides appropriate medical and surgical interventions
  • Family Planning Guidance: Provides valuable information for reproductive decisions
  • Early Intervention: Enables timely management of associated complications
  • Comprehensive Care Coordination: Facilitates multidisciplinary approach to treatment
  • Genetic Counseling Support: Offers professional guidance for patients and families

Understanding Your Test Results

Our comprehensive genetic testing provides detailed results that require professional interpretation:

  • Positive Result: Indicates the presence of a pathogenic FGFR2 mutation consistent with LADD syndrome diagnosis
  • Negative Result: Suggests no detectable FGFR2 mutations, though clinical correlation remains essential
  • Variant of Uncertain Significance (VUS): Identifies genetic changes with unknown clinical impact requiring further evaluation
  • Carrier Status: Determines if individuals carry mutations that could be passed to offspring

All results are accompanied by detailed explanations and recommendations for follow-up care with genetic specialists.

Test Information and Pricing

Test Component Details
Test Name FGFR2 Gene LADD Syndrome NGS Genetic DNA Test
Discount Price $500 USD
Regular Price $700 USD
Turnaround Time 3 to 4 Weeks
Sample Type Blood, Extracted DNA, or One Drop Blood on FTA Card
Specialty Pediatrics
Department Genetics
Method NGS Technology
Disease Type Dysmorphology

Pre-Test Requirements

Before undergoing testing, patients should provide:

  • Complete clinical history relevant to LADD syndrome symptoms
  • Participation in a genetic counseling session
  • Development of a detailed pedigree chart documenting family members affected by FGFR2-related conditions
  • Comprehensive physical examination findings
  • Previous diagnostic test results and imaging studies

Nationwide Testing Availability

We proudly offer the FGFR2 Gene LADD Syndrome NGS Genetic DNA Test at our state-of-the-art facilities across the United States. Our network includes specialized testing centers in major metropolitan areas including New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, San Jose, and numerous other cities. Each location maintains the highest standards of genetic testing excellence and patient care.

Take Control of Your Genetic Health Today

Don’t let uncertainty about genetic conditions affect your quality of life. Our comprehensive FGFR2 Gene LADD Syndrome NGS Genetic DNA Test provides the clarity and answers you need for informed medical decisions. With our discounted price of only $500 USD, advanced genetic testing is more accessible than ever.

Call or WhatsApp us today at +1(267) 388-9828 to schedule your appointment or book your test online. Our genetic specialists are ready to guide you through the testing process and help you understand your results with compassion and expertise.