Sale!

CERS1 Gene Progressive Myoclonus Epilepsy Type 8 Genetic Test

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

-29%

The CERS1 Gene Progressive Myoclonus Epilepsy Type 8 NGS Genetic DNA Test is a cutting-edge diagnostic tool designed to identify mutations in the CERS1 gene associated with progressive myoclonus epilepsy type 8. This comprehensive genetic analysis utilizes next-generation sequencing technology to provide accurate detection of pathogenic variants that cause this rare neurological disorder. The test is particularly valuable for individuals experiencing unexplained myoclonic seizures, progressive neurological decline, or those with a family history of similar symptoms. Results typically take 3-4 weeks and require a simple blood sample or extracted DNA. At only $500 USD, this test offers crucial diagnostic clarity for patients and families affected by this challenging condition, enabling better treatment planning and genetic counseling.

Trusted Testing. Expert Care. Guaranteed Privacy.

  • Accredited and Trusted
  • Expert Scientists, Advanced Technology
  • Data Privacy Guaranteed
Guaranteed Safe Checkout

CERS1 Gene Progressive Myoclonus Epilepsy Type 8 NGS Genetic DNA Test

Comprehensive Genetic Testing for Rare Neurological Disorders

The CERS1 Gene Progressive Myoclonus Epilepsy Type 8 NGS Genetic DNA Test represents a breakthrough in neurological genetic diagnostics. This advanced test specifically targets mutations in the CERS1 gene, which encodes ceramide synthase 1—a crucial enzyme involved in sphingolipid metabolism. Disruptions in this gene lead to progressive myoclonus epilepsy type 8, a rare but devastating neurological condition characterized by progressive neurological deterioration and debilitating seizures.

What This Test Measures and Detects

Our comprehensive NGS-based analysis examines the entire coding region of the CERS1 gene to identify:

  • Pathogenic variants and mutations in the CERS1 gene
  • Single nucleotide polymorphisms (SNPs) associated with disease progression
  • Copy number variations affecting gene function
  • Novel mutations that may not be documented in existing databases
  • Inheritance patterns for family planning purposes

Who Should Consider This Test

This genetic test is particularly recommended for individuals experiencing:

  • Unexplained myoclonic seizures or jerking movements
  • Progressive neurological decline with onset in childhood or adolescence
  • Family history of similar neurological symptoms
  • Diagnostic uncertainty despite extensive neurological evaluation
  • Unexplained ataxia, cognitive decline, or movement disorders
  • Suspected genetic epilepsy syndromes unresponsive to conventional treatments

Key Benefits of Genetic Testing

Undergoing the CERS1 Gene Progressive Myoclonus Epilepsy Type 8 test provides numerous advantages:

  • Accurate Diagnosis: Eliminates diagnostic uncertainty and provides definitive answers
  • Personalized Treatment: Enables targeted therapeutic approaches based on genetic findings
  • Family Planning: Provides crucial information for genetic counseling and reproductive decisions
  • Proactive Management: Allows for early intervention and symptom management strategies
  • Research Contribution: Helps advance scientific understanding of rare neurological disorders

Understanding Your Test Results

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

  • Positive Result: Indicates the presence of a pathogenic CERS1 mutation, confirming the diagnosis of progressive myoclonus epilepsy type 8
  • Negative Result: Suggests that CERS1 mutations are not the cause of symptoms, guiding further diagnostic evaluation
  • Variant of Uncertain Significance: Identifies genetic changes whose clinical significance requires further investigation
  • Carrier Status: Determines if you carry a single copy of a mutation that could be passed to offspring

Test Pricing and Details

Test Feature Details
Test Name CERS1 Gene Progressive Myoclonus Epilepsy Type 8 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 require:

  • Complete clinical history of the patient undergoing testing
  • Genetic counseling session to create a detailed family pedigree chart
  • Documentation of affected family members with similar neurological symptoms
  • Comprehensive neurological evaluation records

Nationwide Accessibility

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, and San Jose. Our network of certified genetic counselors and neurological specialists ensures you receive comprehensive care regardless of your location.

Take the Next Step Toward Clarity

Don’t let diagnostic uncertainty stand in the way of proper treatment and management. Our team of neurological genetics specialists is ready to help you navigate this complex condition. Contact us today to schedule your genetic counseling session and testing appointment.

Call or WhatsApp: +1(267) 388-9828 to book your CERS1 Gene Progressive Myoclonus Epilepsy Type 8 NGS Genetic DNA Test today and take control of your neurological health journey.