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L1CAM Gene Hydrocephalus with Aqueductal Stenosis and Congenital Intestinal Pseudo-obstruction Genetic Test

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

-29%

The L1CAM Gene Hydrocephalus with Aqueductal Stenosis and Congenital Intestinal Pseudo-obstruction NGS Genetic DNA Test is a cutting-edge diagnostic tool that identifies mutations in the L1CAM gene responsible for X-linked hydrocephalus and associated gastrointestinal complications. This comprehensive test utilizes Next-Generation Sequencing (NGS) technology to provide precise genetic analysis for individuals experiencing neurological symptoms, developmental delays, or congenital intestinal issues. The test offers crucial diagnostic information for families with hereditary neurological conditions, enabling early intervention and personalized treatment planning. At $500 USD, this advanced genetic screening provides valuable insights for neurologists and genetic specialists to develop targeted management strategies for affected individuals and their families.

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L1CAM Gene Hydrocephalus with Aqueductal Stenosis and Congenital Intestinal Pseudo-obstruction NGS Genetic DNA Test

Comprehensive Genetic Testing for Neurological and Gastrointestinal Disorders

The L1CAM Gene Hydrocephalus with Aqueductal Stenosis and Congenital Intestinal Pseudo-obstruction NGS Genetic DNA Test represents a significant advancement in diagnostic medicine, offering precise identification of genetic mutations associated with complex neurological and gastrointestinal conditions. This specialized test targets the L1CAM gene, which plays a crucial role in neural development and function.

What Does This Test Measure and Detect?

This advanced genetic screening utilizes Next-Generation Sequencing (NGS) technology to comprehensively analyze the L1CAM gene for mutations that cause:

  • X-linked hydrocephalus with aqueductal stenosis
  • Congenital intestinal pseudo-obstruction
  • Neural development abnormalities
  • Genetic variants affecting cell adhesion molecules
  • Inherited neurological disorders

The test provides detailed analysis of specific genetic markers that are responsible for the disruption of normal cerebrospinal fluid flow and gastrointestinal motility, offering clinicians valuable diagnostic information for treatment planning.

Who Should Consider This Test?

This genetic test is recommended for individuals presenting with the following symptoms or family history:

  • Infants and children with unexplained hydrocephalus
  • Patients with aqueductal stenosis of unknown origin
  • Individuals with congenital intestinal motility disorders
  • Family members of individuals diagnosed with L1CAM-related disorders
  • Patients with developmental delays and neurological symptoms
  • Those with a family history of X-linked neurological conditions
  • Individuals experiencing chronic gastrointestinal dysfunction

Clinical Benefits of Genetic Testing

Undergoing the L1CAM gene test provides numerous advantages for patients and healthcare providers:

  • Accurate Diagnosis: Provides definitive genetic confirmation of L1CAM-related disorders
  • Early Intervention: Enables timely medical management and treatment planning
  • Family Planning: Offers valuable information for genetic counseling and reproductive decisions
  • Personalized Treatment: Guides development of targeted therapeutic approaches
  • Prognostic Information: Helps predict disease progression and potential complications
  • Research Contribution: Contributes to scientific understanding of neurological disorders

Understanding Your Test Results

Our comprehensive genetic counseling services help patients interpret their test results effectively:

  • Positive Result: Indicates the presence of L1CAM gene mutation, confirming diagnosis
  • Negative Result: Suggests absence of tested mutations, though other genetic factors may be involved
  • Variant of Unknown Significance: Identifies genetic changes requiring further investigation
  • Carrier Status: Determines if individuals carry the mutation without showing symptoms

All results are accompanied by detailed explanations from our certified genetic counselors, ensuring patients fully understand their genetic profile and its implications.

Test Pricing Information

Price Type Amount (USD)
Discount Price $500
Regular Price $700

Nationwide Testing Availability

We proudly offer comprehensive genetic testing services across the United States, with convenient locations in all major metropolitan areas including:

  • New York City and surrounding areas
  • Los Angeles and Southern California
  • Chicago and the Midwest region
  • Houston and Texas metropolitan areas
  • Miami and Florida locations
  • Seattle and Pacific Northwest centers
  • Boston and New England facilities
  • Atlanta and Southeastern regions

Test Specifications

  • 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
  • Specialty: Neurology and Genetics
  • Department: Genetics
  • Disease Type: Neurological Disorders

Pre-Test Requirements

Before undergoing testing, patients should provide:

  • Complete clinical history documentation
  • Participation in genetic counseling session
  • Detailed pedigree chart of affected family members
  • Relevant medical records and previous test results

Take Control of Your Genetic Health Today

Don’t let uncertainty about neurological symptoms affect your quality of life. Our advanced L1CAM gene testing provides the clarity you need for informed medical decisions and personalized treatment approaches. With convenient locations nationwide and comprehensive genetic counseling support, we make advanced genetic testing accessible to everyone.

Call or WhatsApp us today at +1(267) 388-9828 to schedule your genetic counseling session and book your L1CAM Gene Hydrocephalus with Aqueductal Stenosis and Congenital Intestinal Pseudo-obstruction NGS Genetic DNA Test.

Our team of certified genetic specialists is ready to guide you through the testing process, answer your questions, and provide the expert care you deserve. Take the first step toward understanding your genetic health and securing better medical outcomes for you and your family.