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KCNJ10 Gene SESAME Syndrome Genetic Test

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

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The KCNJ10 Gene SESAME Syndrome NGS Genetic DNA Test is a comprehensive genetic screening that identifies mutations in the KCNJ10 gene associated with SESAME syndrome, a rare neurological disorder. This advanced test utilizes Next-Generation Sequencing (NGS) technology to provide accurate detection of genetic variations that cause seizures, sensorineural deafness, ataxia, mental retardation, and electrolyte imbalance. The test is crucial for individuals experiencing unexplained neurological symptoms, developmental delays, or with family history of similar conditions. At only $500 USD, this test offers early diagnosis, personalized treatment planning, and genetic counseling guidance. Results are typically available within 3-4 weeks, providing valuable insights for managing this complex neurological condition.

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KCNJ10 Gene SESAME Syndrome NGS Genetic DNA Test

Comprehensive Genetic Screening for Neurological Disorders

The KCNJ10 Gene SESAME Syndrome NGS Genetic DNA Test represents a breakthrough in neurological genetic testing, offering precise detection of mutations associated with SESAME syndrome (Seizures, Sensorineural deafness, Ataxia, Mental retardation, and Electrolyte imbalance). This advanced diagnostic tool utilizes cutting-edge Next-Generation Sequencing technology to provide comprehensive analysis of the KCNJ10 gene, enabling early detection and personalized management strategies for affected individuals and families.

What Does This Test Measure and Detect?

This specialized genetic test specifically targets the KCNJ10 gene, which encodes an inwardly rectifying potassium channel crucial for maintaining proper neurological function and electrolyte balance. The test detects:

  • Pathogenic variants and mutations in the KCNJ10 gene
  • Single nucleotide polymorphisms associated with SESAME syndrome
  • Copy number variations affecting gene function
  • Novel genetic alterations impacting potassium channel regulation

Who Should Consider This Genetic Test?

This test is recommended for individuals presenting with the following symptoms or clinical indications:

  • Unexplained seizures or epilepsy, particularly in childhood
  • Progressive sensorineural hearing loss
  • Ataxia or coordination difficulties
  • Developmental delays or intellectual disability
  • Electrolyte imbalances, especially hypomagnesemia and hypokalemia
  • Family history of similar neurological symptoms
  • Suspected inherited neurological disorders
  • Unexplained neurological symptoms in multiple family members

Key Benefits of KCNJ10 Genetic Testing

Undergoing this comprehensive genetic analysis provides numerous advantages for patients and healthcare providers:

  • Early and Accurate Diagnosis: Enables precise identification of SESAME syndrome, reducing diagnostic uncertainty
  • Personalized Treatment Planning: Guides targeted therapeutic interventions based on specific genetic findings
  • Family Planning Guidance: Provides crucial information for genetic counseling and reproductive decisions
  • Proactive Management: Allows for early intervention and monitoring of potential complications
  • Genetic Risk Assessment: Helps determine recurrence risks for family members
  • Comprehensive Neurological Evaluation: Integrates genetic findings with clinical presentation for holistic care

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:

  • Positive Result: Indicates the presence of pathogenic variants in the KCNJ10 gene, confirming SESAME syndrome diagnosis
  • Negative Result: Suggests no disease-causing mutations were detected, though clinical correlation is essential
  • Variant of Uncertain Significance: Identifies genetic changes whose clinical significance requires further investigation
  • Comprehensive Interpretation: Detailed explanation of findings and their clinical implications
  • Management Recommendations: Personalized guidance for treatment and monitoring strategies

Test Pricing and Availability

Test Name Regular Price Discount Price
KCNJ10 Gene SESAME Syndrome NGS Genetic DNA Test $700 USD $500 USD

Nationwide Testing Availability

We proudly offer comprehensive genetic testing services across the United States, with convenient locations in all major metropolitan areas including New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, and San Jose. Our state-of-the-art laboratories ensure consistent, high-quality testing regardless of your location.

Pre-Test Requirements and Sample Collection

Before scheduling your test, please ensure you have:

  • Complete clinical history documentation
  • Genetic counseling session completed
  • Family pedigree chart prepared
  • Appropriate sample type selected (Blood, Extracted DNA, or One drop Blood on FTA Card)

Our genetic testing process is designed for maximum convenience and accuracy, with results typically available within 3-4 weeks from sample receipt.

Take Control of Your Neurological Health Today

Don’t let uncertainty about neurological symptoms affect your quality of life. The KCNJ10 Gene SESAME Syndrome NGS Genetic DNA Test provides the clarity and answers you need for informed healthcare decisions. Our team of genetic specialists and neurologists is ready to support you through every step of the testing process.

Ready to schedule your genetic test? Contact our genetic counseling team today at +1(267) 388-9828 or book your appointment online. Take the first step toward understanding your neurological health with confidence and precision.