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BRAT1 Gene Neurodevelopmental Disorder with Cerebellar Atrophy Genetic Test

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

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The BRAT1 Gene Neurodevelopmental Disorder with Cerebellar Atrophy NGS Genetic DNA Test is a comprehensive diagnostic tool that identifies mutations in the BRAT1 gene associated with severe neurological conditions. This advanced next-generation sequencing test detects genetic variations responsible for neurodevelopmental disorders characterized by cerebellar atrophy, seizures, and developmental delays. Priced at $500 USD (regularly $700), this test provides crucial information for accurate diagnosis, enabling targeted treatment strategies and genetic counseling. Early detection through this specialized DNA analysis helps families understand inherited neurological conditions and make informed healthcare decisions.

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BRAT1 Gene Neurodevelopmental Disorder with Cerebellar Atrophy NGS Genetic DNA Test

Comprehensive Genetic Testing for Neurological Conditions

The BRAT1 Gene Neurodevelopmental Disorder with Cerebellar Atrophy NGS Genetic DNA Test represents a breakthrough in neurological genetic diagnostics. This specialized test utilizes cutting-edge Next-Generation Sequencing (NGS) technology to identify mutations in the BRAT1 gene, which plays a critical role in brain development and neurological function. Early and accurate detection of BRAT1 gene mutations is essential for proper diagnosis, treatment planning, and genetic counseling for affected individuals and their families.

What Does This Test Measure and Detect?

This advanced genetic test specifically targets the BRAT1 gene, analyzing its complete coding sequence to identify:

  • Pathogenic variants and mutations in the BRAT1 gene
  • Single nucleotide polymorphisms (SNPs) associated with neurological disorders
  • Copy number variations affecting gene function
  • Novel genetic alterations linked to cerebellar atrophy
  • Inheritance patterns of neurological conditions

Who Should Consider This Test?

This specialized genetic test is recommended for individuals presenting with:

  • Unexplained neurodevelopmental delays in infancy or childhood
  • Cerebellar atrophy detected through brain imaging studies
  • Recurrent seizures or epilepsy of unknown origin
  • Family history of neurological disorders
  • Progressive motor function deterioration
  • Developmental regression in early childhood
  • Multiple family members with similar neurological symptoms

Clinical Benefits of BRAT1 Genetic Testing

Undergoing BRAT1 genetic testing provides numerous clinical advantages:

  • Accurate Diagnosis: Confirms or rules out BRAT1-related neurological disorders
  • Personalized Treatment: Enables targeted therapeutic approaches based on genetic findings
  • Family Planning: Provides crucial information for genetic counseling and reproductive decisions
  • Prognostic Information: Helps predict disease progression and potential complications
  • Early Intervention: Facilitates timely implementation of supportive therapies
  • Research Contribution: Advances understanding of rare neurological conditions

Understanding Your Test Results

Our comprehensive genetic counseling services help you interpret your BRAT1 test results:

  • Positive Result: Indicates the presence of BRAT1 gene mutation, confirming diagnosis and guiding treatment strategies
  • Negative Result: Suggests absence of detectable BRAT1 mutations, though other genetic causes may need investigation
  • Variant of Uncertain Significance: Requires additional family studies and clinical correlation
  • Carrier Status: Identifies individuals who may pass the condition to offspring

Test Details and Pricing

Test Parameter Details
Test Name BRAT1 Gene Neurodevelopmental Disorder with Cerebellar Atrophy 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 Requirements

Before undergoing BRAT1 genetic testing, patients should provide:

  • Complete clinical history and neurological examination findings
  • Genetic counseling session to create detailed family pedigree chart
  • Documentation of affected family members with similar symptoms
  • Previous neurological test results and brain imaging studies

Nationwide Testing Availability

We have comprehensive testing facilities across the United States, with branches 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 ensures convenient access to advanced genetic testing services regardless of your location.

Take the Next Step Toward Diagnosis

Don’t let uncertainty about neurological symptoms delay proper diagnosis and treatment. Our BRAT1 Gene Neurodevelopmental Disorder with Cerebellar Atrophy NGS Genetic DNA Test provides the clarity needed for effective medical management. Schedule your test today and take control of your neurological health.

Call or WhatsApp us now at +1(267) 388-9828 to book your appointment or get more information about this specialized genetic test.