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VLDLR Gene Cerebellar Hypoplasia and Mental Retardation with or without Quadrupedal Locomotion Type 1 Genetic Test

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

-29%

The VLDLR Gene Cerebellar Hypoplasia and Mental Retardation with or without Quadrupedal Locomotion Type 1 NGS Genetic DNA Test is a comprehensive diagnostic tool that identifies mutations in the VLDLR gene responsible for this rare neurological disorder. This advanced next-generation sequencing test detects genetic abnormalities that cause cerebellar hypoplasia, intellectual disability, and the distinctive quadrupedal locomotion pattern. The test provides crucial diagnostic information for individuals presenting with developmental delays, balance issues, and neurological symptoms. For just $500 USD, patients receive definitive genetic confirmation, enabling accurate diagnosis and personalized treatment planning. This test is essential for families with a history of neurological disorders and individuals experiencing unexplained developmental challenges.

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VLDLR Gene Cerebellar Hypoplasia and Mental Retardation with or without Quadrupedal Locomotion Type 1 NGS Genetic DNA Test

Comprehensive Genetic Testing for Neurological Disorders

The VLDLR Gene Cerebellar Hypoplasia and Mental Retardation with or without Quadrupedal Locomotion Type 1 NGS Genetic DNA Test represents a breakthrough in neurological genetic diagnostics. This sophisticated test utilizes next-generation sequencing technology to identify mutations in the VLDLR (Very Low-Density Lipoprotein Receptor) gene, which plays a critical role in brain development and function. The VLDLR gene encodes a receptor involved in the Reelin signaling pathway, essential for proper neuronal migration and cerebellar formation during embryonic development.

What This Advanced Genetic Test Measures

Our comprehensive NGS genetic test specifically targets and analyzes the VLDLR gene to detect:

  • Point mutations and single nucleotide variants affecting VLDLR function
  • Insertions and deletions that disrupt normal gene expression
  • Splice site mutations impacting protein production
  • Copy number variations affecting gene dosage
  • Pathogenic variants associated with cerebellar hypoplasia

Who Should Consider VLDLR Genetic Testing?

Clinical Indications and Symptoms

This specialized genetic test is recommended for individuals presenting with:

  • Developmental delay and intellectual disability of unknown origin
  • Cerebellar hypoplasia identified through brain imaging
  • Balance and coordination difficulties from early childhood
  • Distinctive quadrupedal locomotion pattern
  • Family history of similar neurological symptoms
  • Unexplained ataxia or movement disorders
  • Speech and language development delays
  • Abnormal gait and motor function impairment

Significant Benefits of VLDLR Genetic Testing

Undergoing this comprehensive genetic analysis provides multiple advantages:

  • Definitive Diagnosis: Obtain conclusive genetic confirmation of VLDLR-related disorders
  • Family Planning Guidance: Understand inheritance patterns for future family planning
  • Personalized Treatment: Enable targeted interventions and management strategies
  • Early Intervention: Facilitate timely therapeutic approaches for better outcomes
  • Genetic Counseling: Provide accurate information for affected families
  • Research Contribution: Contribute to advancing knowledge of rare neurological conditions

Understanding Your Test Results

Interpretation and Clinical Implications

Our genetic specialists provide comprehensive result interpretation:

  • Positive Result: Identifies pathogenic VLDLR mutations confirming diagnosis
  • Negative Result: Rules out VLDLR-related disorders, suggesting alternative diagnoses
  • Variant of Uncertain Significance: Requires additional family studies and clinical correlation
  • Carrier Status: Identifies individuals who may pass the condition to offspring

Test Pricing and Availability

Test Description Regular Price Discount Price
VLDLR Gene Cerebellar Hypoplasia and Mental Retardation with or without Quadrupedal Locomotion Type 1 NGS Genetic DNA Test $700 USD $500 USD

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
  • Disease Category: Neurological Disorders

Pre-Test Requirements

Before scheduling your VLDLR genetic test, we recommend:

  • Complete clinical history documentation
  • Genetic counseling session with our specialists
  • Family pedigree chart development
  • Discussion of testing implications and expectations

Nationwide Testing Availability

We proudly serve patients across the United States with convenient testing locations in all major cities including New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, San Jose, and many more. Our network of certified genetic testing facilities ensures accessibility and convenience for patients nationwide.

Take the Next Step Toward Genetic Clarity

Don’t let uncertainty about neurological symptoms affect your quality of life. Our VLDLR genetic test provides the answers you need for proper diagnosis and management. With our discounted price of $500 USD and comprehensive genetic analysis, you can gain valuable insights into your neurological health.

Ready to schedule your test? Contact our genetic specialists today at +1(267) 388-9828 or book your appointment online. Take control of your neurological health with definitive genetic testing from America’s leading genetics laboratory.