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SNAP29 Gene Cerebral Dysgenesis Neuropathy Ichthyosis Palmoplantar Keratoderma Syndrome NGS Genetic DNA Test

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

-29%

The SNAP29 Gene Cerebral Dysgenesis Neuropathy Ichthyosis Palmoplantar Keratoderma Syndrome NGS Genetic DNA Test is a comprehensive diagnostic tool that identifies mutations in the SNAP29 gene responsible for this rare genetic disorder. Using next-generation sequencing (NGS) technology, this test provides precise detection of genetic variants associated with cerebral malformations, neurological complications, skin abnormalities, and palmoplantar keratoderma. The test is essential for individuals presenting with developmental delays, neurological symptoms, ichthyosis, and thickened skin on palms and soles. At only $500 USD, this advanced genetic analysis offers crucial information for accurate diagnosis, family planning decisions, and personalized medical management strategies.

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SNAP29 Gene Cerebral Dysgenesis Neuropathy Ichthyosis Palmoplantar Keratoderma Syndrome NGS Genetic DNA Test

Comprehensive Genetic Analysis for Rare Neurological and Dermatological Disorders

The SNAP29 Gene Cerebral Dysgenesis Neuropathy Ichthyosis Palmoplantar Keratoderma Syndrome NGS Genetic DNA Test represents a cutting-edge diagnostic approach for identifying mutations in the SNAP29 gene, which plays a critical role in cellular membrane fusion and neurotransmitter release. This comprehensive genetic analysis utilizes next-generation sequencing technology to provide accurate detection of pathogenic variants associated with this complex multisystem disorder.

What Does This Test Measure and Detect?

This advanced genetic test specifically targets the SNAP29 gene, which encodes a protein essential for proper synaptic function and cellular membrane dynamics. The test detects:

  • Pathogenic mutations in the SNAP29 gene associated with cerebral dysgenesis
  • Genetic variants linked to peripheral neuropathy development
  • Mutations causing ichthyosis and palmoplantar keratoderma
  • Both inherited and de novo genetic alterations
  • Single nucleotide variants, insertions, deletions, and copy number variations

Who Should Consider This Genetic Test?

This test is recommended for individuals presenting with the following symptoms or clinical indications:

  • Infants and children with developmental delays and cerebral malformations
  • Patients exhibiting neurological symptoms including neuropathy and seizures
  • Individuals with congenital ichthyosis or severe skin scaling
  • Those presenting with palmoplantar keratoderma (thickened skin on palms and soles)
  • Family members of individuals diagnosed with SNAP29-related disorders
  • Couples with family history planning pregnancy
  • Patients with unexplained multisystem involvement affecting brain, nerves, and skin

Key Benefits of SNAP29 Genetic Testing

Undergoing this comprehensive genetic analysis provides numerous clinical advantages:

  • Accurate Diagnosis: Confirms or rules out SNAP29-related disorders with high precision
  • Personalized Treatment: Enables targeted therapeutic approaches based on genetic findings
  • Family Planning: Provides crucial information for reproductive decision-making
  • Prognostic Insights: Helps predict disease progression and potential complications
  • Early Intervention: Facilitates timely management strategies for better outcomes
  • Genetic Counseling: Supports informed discussions about inheritance patterns

Understanding Your Test Results

Our comprehensive genetic counseling services help you interpret your results effectively:

  • Positive Result: Indicates the presence of pathogenic SNAP29 mutations, confirming diagnosis and guiding management
  • Negative Result: Suggests absence of detectable SNAP29 mutations, though clinical correlation remains essential
  • Variant of Uncertain Significance: Requires additional family studies and clinical evaluation
  • Carrier Status: Identifies individuals who may pass the condition to offspring

Test Pricing and Details

Test Component Details
Test Name SNAP29 Gene Cerebral Dysgenesis Neuropathy Ichthyosis Palmoplantar Keratoderma Syndrome 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

Nationwide Accessibility

We have conveniently located branches across the United States, including major metropolitan areas such as New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, and San Jose. Our state-of-the-art facilities ensure consistent quality and reliable results nationwide.

Take the Next Step Toward Genetic Clarity

Don’t let uncertainty about genetic conditions affect your health decisions. Our expert genetic counselors and medical professionals are ready to guide you through the testing process and help you understand your results. Schedule your SNAP29 genetic test today to gain valuable insights into your genetic health.

Call or WhatsApp us now at +1(267) 388-9828 to book your appointment or discuss your testing options with our genetic specialists.

Early genetic diagnosis can make a significant difference in managing complex neurological and dermatological conditions. Trust our expertise in genetic testing to provide the answers you need for informed healthcare decisions.