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TIMM8A Gene Jensen Syndrome Genetic Test

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

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The TIMM8A Gene Jensen Syndrome NGS Genetic DNA Test is a specialized diagnostic tool that identifies mutations in the TIMM8A gene associated with Jensen syndrome, a rare X-linked neurological disorder. This comprehensive next-generation sequencing test provides accurate detection of genetic variations responsible for progressive sensorineural hearing loss, dystonia, and cognitive impairment. Priced at $500 USD, this advanced genetic analysis helps confirm diagnosis, guide treatment decisions, and provide crucial information for family planning. The test requires a simple blood sample or extracted DNA and delivers results within 3-4 weeks, supported by professional genetic counseling services.

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TIMM8A Gene Jensen Syndrome NGS Genetic DNA Test

Comprehensive Genetic Testing for Rare Neurological Disorders

The TIMM8A Gene Jensen Syndrome NGS Genetic DNA Test represents a breakthrough in neurological genetic diagnostics, offering precise identification of mutations responsible for Jensen syndrome. This rare X-linked disorder affects mitochondrial function and manifests through progressive neurological symptoms that significantly impact quality of life. Our advanced testing methodology provides families and healthcare providers with definitive answers for complex neurological presentations.

What This Test Measures and Detects

This specialized genetic test utilizes next-generation sequencing (NGS) technology to comprehensively analyze the TIMM8A gene, also known as the DDP1 gene. The test specifically identifies:

  • Point mutations, deletions, and insertions in the TIMM8A gene
  • Variants associated with impaired mitochondrial protein import
  • Genetic markers for Mohr-Tranebjaerg syndrome (deafness-dystonia syndrome)
  • X-linked inheritance patterns affecting male patients predominantly
  • Mutations impacting the mitochondrial intermembrane space

Who Should Consider This Test

This genetic test is recommended for individuals presenting with symptoms suggestive of Jensen syndrome or related mitochondrial disorders:

  • Progressive sensorineural hearing loss beginning in childhood
  • Development of dystonia or movement disorders
  • Cognitive impairment or intellectual disability
  • Visual disturbances including cortical blindness
  • Family history of X-linked neurological disorders
  • Unexplained neurological symptoms in male patients
  • Suspected mitochondrial dysfunction syndromes

Clinical Benefits of Genetic Testing

Undergoing the TIMM8A Gene Jensen Syndrome NGS Genetic DNA Test provides numerous advantages for patients and families:

  • Definitive Diagnosis: Confirms or rules out Jensen syndrome with high accuracy
  • Treatment Guidance: Informs appropriate management strategies for neurological symptoms
  • Genetic Counseling: Provides essential information for family planning decisions
  • Early Intervention: Enables proactive management of progressive symptoms
  • Family Risk Assessment: Identifies carrier status in female relatives
  • Research Contribution: Advances understanding of rare neurological conditions

Understanding Your Test Results

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

  • Positive Result: Indicates the presence of a pathogenic TIMM8A mutation, confirming Jensen syndrome diagnosis
  • Negative Result: Suggests Jensen syndrome is unlikely, though other genetic conditions may need consideration
  • Variant of Uncertain Significance: Identifies genetic changes requiring further clinical correlation
  • Carrier Status: For female relatives, indicates risk of passing the condition to offspring

All results include detailed explanations and recommendations for next steps, supported by our team of genetic specialists.

Test Pricing and Details

Test Component Details
Test Name TIMM8A Gene Jensen Syndrome 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

To ensure optimal testing outcomes, we recommend:

  • Complete clinical history documentation
  • Genetic counseling session prior to testing
  • Development of detailed family pedigree chart
  • Review of neurological examination findings
  • Discussion of testing implications with healthcare provider

Nationwide Testing Availability

We proudly serve patients across the United States with convenient testing locations in all major metropolitan areas including New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, San Jose, and many more. Our network of certified collection centers ensures accessible genetic testing services nationwide.

Take the Next Step Toward Answers

Don’t let uncertainty about neurological symptoms continue. Our expert team of genetic specialists and neurologists is ready to provide the comprehensive testing and support you need. Schedule your TIMM8A Gene Jensen Syndrome NGS Genetic DNA Test today and take control of your neurological health.

Call or WhatsApp us now at +1(267) 388-9828 to book your test or request more information about our genetic testing services.

Our dedicated patient care coordinators are available to answer your questions, discuss insurance coverage options, and help you begin your journey toward accurate diagnosis and effective management of neurological conditions.