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RAB3GAP1 Gene Warburg Micro Syndrome Type 1 Genetic Test

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

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The RAB3GAP1 Gene Warburg Micro Syndrome Type 1 NGS Genetic DNA Test is a comprehensive genetic analysis designed to detect mutations in the RAB3GAP1 gene associated with Warburg Micro Syndrome Type 1. This rare autosomal recessive neurological disorder affects brain development, vision, and motor function. Using Next-Generation Sequencing (NGS) technology, this test provides precise identification of pathogenic variants that cause this severe condition. The test is particularly valuable for families with a history of developmental delays, congenital cataracts, microcephaly, or other neurological symptoms. Early genetic diagnosis enables better medical management, informed family planning decisions, and access to specialized care. The test costs $500 USD and provides results within 3-4 weeks, offering crucial insights for affected individuals and their families.

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RAB3GAP1 Gene Warburg Micro Syndrome Type 1 NGS Genetic DNA Test

Comprehensive Genetic Testing for Rare Neurological Disorders

The RAB3GAP1 Gene Warburg Micro Syndrome Type 1 NGS Genetic DNA Test represents a cutting-edge diagnostic approach for identifying mutations associated with Warburg Micro Syndrome Type 1, a rare autosomal recessive neurological condition. This sophisticated genetic analysis utilizes Next-Generation Sequencing technology to provide comprehensive insights into the RAB3GAP1 gene, which plays a critical role in neurological development and function.

What This Test Detects and Measures

This advanced genetic test specifically targets the RAB3GAP1 gene, analyzing it for pathogenic variants that cause Warburg Micro Syndrome Type 1. The test examines:

  • Point mutations, insertions, and deletions in the RAB3GAP1 gene
  • Autosomal recessive inheritance patterns
  • Pathogenic variants affecting neurological development
  • Genetic markers associated with microcephaly and developmental delays
  • Mutations impacting visual and motor function development

Who Should Consider This Genetic Test

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

  • Infants and children with congenital cataracts or severe visual impairment
  • Individuals with microcephaly (abnormally small head size)
  • Patients experiencing significant developmental delays
  • Families with a history of neurological disorders
  • Couples with previous affected children planning future pregnancies
  • Individuals with hypotonia (reduced muscle tone) and motor function issues
  • Patients with corpus callosum abnormalities detected in brain imaging

Key Benefits of Genetic Testing

Undergoing the RAB3GAP1 Gene Warburg Micro Syndrome Type 1 NGS Genetic DNA Test provides numerous advantages:

  • Accurate Diagnosis: Provides definitive genetic confirmation of Warburg Micro Syndrome Type 1
  • Family Planning Guidance: Enables informed reproductive decisions for at-risk families
  • Early Intervention: Facilitates timely medical management and therapeutic interventions
  • Genetic Counseling: Supports comprehensive family genetic risk assessment
  • Research Contribution: Contributes to ongoing medical research on rare neurological disorders
  • Peace of Mind: Provides clarity and understanding of the genetic basis of symptoms

Understanding Your Test Results

Your genetic test results will be carefully interpreted by our team of certified genetic counselors and neurologists. The report will include:

  • Detailed analysis of identified genetic variants
  • Clinical significance of any detected mutations
  • Inheritance pattern explanation
  • Recommendations for medical follow-up and management
  • Family testing guidance when applicable
  • Access to genetic counseling services for result interpretation

Test Pricing and Details

Test Feature Details
Test Name RAB3GAP1 Gene Warburg Micro Syndrome Type 1 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
Testing Method Next-Generation Sequencing (NGS) Technology

Pre-Test Preparation Requirements

To ensure optimal testing conditions and accurate results, please prepare the following:

  • Complete clinical history documentation of the patient
  • Genetic counseling session to create a detailed family pedigree chart
  • Information about family members affected with similar neurological symptoms
  • Previous medical records and diagnostic reports

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 family’s future. Our comprehensive RAB3GAP1 Gene Warburg Micro Syndrome Type 1 NGS Genetic DNA Test provides the answers you need for informed medical decisions and family planning. Our team of genetic specialists is ready to guide you through the testing process and provide compassionate support every step of the way.

Book your genetic test today by calling our dedicated genetic counseling team at +1(267) 388-9828 or schedule your appointment online. Take control of your genetic health and gain the clarity you deserve.