Sale!

CLN6 Gene Ceroid Lipofuscinosis Neuronal Type 6 Genetic Test

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

-29%

The CLN6 Gene Ceroid Lipofuscinosis Neuronal Type 6 NGS Genetic DNA Test is a comprehensive diagnostic tool that identifies mutations in the CLN6 gene responsible for Batten disease, a rare inherited neurodegenerative disorder. This advanced next-generation sequencing test provides precise detection of genetic variants that cause progressive neurological deterioration in children and young adults. The test is crucial for families with a history of ceroid lipofuscinosis or children showing symptoms like vision loss, seizures, and cognitive decline. Early diagnosis through this $500 USD test enables better disease management, family planning decisions, and access to specialized care. Our NGS technology offers superior accuracy in detecting CLN6 mutations, helping physicians develop targeted treatment strategies and providing families with definitive answers about this challenging condition.

Trusted Testing. Expert Care. Guaranteed Privacy.

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

CLN6 Gene Ceroid Lipofuscinosis Neuronal Type 6 NGS Genetic DNA Test

Comprehensive Genetic Testing for Batten Disease

The CLN6 Gene Ceroid Lipofuscinosis Neuronal Type 6 NGS Genetic DNA Test represents a breakthrough in diagnostic precision for families affected by Batten disease, a rare inherited neurodegenerative disorder. This advanced genetic test utilizes next-generation sequencing technology to identify mutations in the CLN6 gene, which plays a critical role in cellular waste management within neurons. Early and accurate diagnosis is essential for managing this progressive condition that primarily affects children and young adults.

What This Test Measures and Detects

Our CLN6 genetic test specifically targets and analyzes the CLN6 gene located on chromosome 15q21-q23. The test identifies:

  • Pathogenic variants and mutations in the CLN6 gene
  • Single nucleotide polymorphisms associated with neuronal ceroid lipofuscinosis type 6
  • Deletions, insertions, and missense mutations affecting protein function
  • Compound heterozygous and homozygous mutations
  • Novel variants of uncertain significance with detailed interpretation

Who Should Consider This Genetic Test

This test is recommended for individuals displaying symptoms or with family history suggesting CLN6-related disorders:

  • Children experiencing progressive vision loss starting between ages 18 months and 8 years
  • Patients with developmental regression and loss of previously acquired skills
  • Individuals with seizure disorders that are difficult to control with medication
  • Children showing cognitive decline and behavioral changes
  • Patients with motor coordination difficulties and speech impairment
  • Families with a history of Batten disease or similar neurodegenerative conditions
  • Couples planning pregnancy with known family history of neuronal ceroid lipofuscinosis

Key Benefits of CLN6 Genetic Testing

Choosing our comprehensive CLN6 genetic test provides numerous advantages:

  • Early Intervention: Enables timely medical management and symptom control
  • Family Planning: Provides crucial information for reproductive decisions
  • Accurate Diagnosis: Eliminates diagnostic uncertainty and misdiagnosis
  • Treatment Guidance: Helps physicians develop targeted care plans
  • Genetic Counseling: Supports families in understanding inheritance patterns
  • Research Contribution: Advances scientific understanding of Batten disease

Understanding Your Test Results

Our comprehensive genetic report provides clear interpretation of your CLN6 gene analysis:

  • Positive Result: Indicates presence of known pathogenic mutations, confirming diagnosis of CLN6-related neuronal ceroid lipofuscinosis
  • Negative Result: Suggests absence of detectable CLN6 mutations, though other genetic causes should be considered
  • Variant of Uncertain Significance: Identifies genetic changes with unknown clinical impact, requiring further evaluation
  • Carrier Status: Determines if individuals carry one copy of a mutated gene without showing symptoms

All results include detailed explanations and recommendations for follow-up care with genetic specialists.

Test Pricing and Details

Test Feature Details
Test Name CLN6 Gene Ceroid Lipofuscinosis Neuronal Type 6 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

Nationwide Testing Availability

We have diagnostic centers conveniently located across the United States, serving patients in all major metropolitan areas including New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, San Jose, and many other cities. Our network of certified genetic counselors and medical professionals ensures you receive comprehensive support throughout the testing process.

Take the Next Step Toward Answers

If you or your loved one is experiencing symptoms suggestive of CLN6-related disorders, don’t wait to get definitive answers. Our advanced genetic testing provides the clarity needed for proper diagnosis and management. Contact our genetic specialists today to schedule your test and begin your journey toward understanding and managing this complex condition.

Call or WhatsApp us now at +1(267) 388-9828 to book your CLN6 genetic test and take control of your health journey.