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KRIT1 Gene Cerebral Cavernous Malformations Type 1 NGS Genetic DNA Test

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

-29%

The KRIT1 Gene Cerebral Cavernous Malformations Type 1 NGS Genetic DNA Test is a cutting-edge genetic analysis that identifies mutations in the KRIT1 gene associated with cerebral cavernous malformations (CCM1). This comprehensive test utilizes Next-Generation Sequencing (NGS) technology to detect hereditary vascular abnormalities in the brain that can cause seizures, hemorrhages, and neurological symptoms. The test is crucial for individuals with family history of CCM1, unexplained neurological symptoms, or those planning pregnancy with known family risk factors. Results provide valuable information for medical management, treatment planning, and family genetic counseling. The test is available for $500 USD with a regular price of $700 USD, offering significant savings for comprehensive genetic screening.

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KRIT1 Gene Cerebral Cavernous Malformations Type 1 NGS Genetic DNA Test

Comprehensive Genetic Testing for Hereditary Brain Vascular Malformations

The KRIT1 Gene Cerebral Cavernous Malformations Type 1 NGS Genetic DNA Test represents a breakthrough in genetic diagnostics for individuals at risk of hereditary cerebrovascular disorders. This advanced genetic screening utilizes state-of-the-art Next-Generation Sequencing (NGS) technology to identify mutations in the KRIT1 gene, which is directly associated with Cerebral Cavernous Malformations Type 1 (CCM1) – a serious condition characterized by abnormal blood vessel clusters in the brain and spinal cord.

What This Test Measures and Detects

Our comprehensive NGS genetic analysis specifically targets the KRIT1 gene (also known as CCM1), which plays a critical role in maintaining the structural integrity of blood vessels in the central nervous system. The test identifies:

  • Pathogenic variants and mutations in the KRIT1 gene
  • Single nucleotide polymorphisms (SNPs) associated with CCM1
  • Deletion and duplication events affecting gene function
  • Inheritance patterns for family genetic counseling
  • Risk assessment for cerebral cavernous malformation development

Who Should Consider This Genetic Test

This specialized genetic test is recommended for individuals experiencing or concerned about:

  • Family History: Individuals with known family history of cerebral cavernous malformations
  • Neurological Symptoms: Unexplained seizures, headaches, or neurological deficits
  • Previous Diagnosis: Patients diagnosed with cerebral cavernous malformations seeking genetic confirmation
  • Family Planning: Couples planning pregnancy with family history of CCM1
  • Asymptomatic Screening: Individuals from families with known KRIT1 mutations
  • Recurrent Symptoms: Multiple episodes of unexplained neurological events

Key Benefits of KRIT1 Genetic Testing

  • Early Risk Identification: Detect genetic predisposition before symptom onset
  • Personalized Medical Management: Tailor monitoring and treatment strategies
  • Family Planning Guidance: Make informed reproductive decisions
  • Proactive Health Monitoring: Implement appropriate surveillance protocols
  • Genetic Counseling Support: Comprehensive family risk assessment
  • Treatment Optimization: Guide surgical and medical intervention decisions

Understanding Your Test Results

Your genetic test results will be carefully analyzed and presented with comprehensive interpretation:

  • Positive Result: Indicates presence of KRIT1 gene mutation, confirming increased risk for CCM1 development
  • Negative Result: No detected mutation, significantly reducing hereditary risk
  • Variant of Uncertain Significance: Genetic changes requiring further clinical correlation
  • Carrier Status: Information relevant for family planning and genetic counseling

All results include detailed explanations and recommendations for next steps, including consultation with our genetic specialists and neurologists for comprehensive care planning.

Test Pricing and Details

Test Component Details Price (USD)
Test Name KRIT1 Gene Cerebral Cavernous Malformations Type 1 NGS Genetic DNA Test
Discount Price Limited Time Special Offer $500
Regular Price Standard Pricing $700
Turnaround Time Comprehensive Analysis Period 3-4 Weeks
Sample Type Blood, Extracted DNA, or Blood on FTA Card
Technology Next-Generation Sequencing (NGS)

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, reliable results regardless of your location.

Take Control of Your Genetic Health Today

Don’t let uncertainty about hereditary vascular conditions affect your health decisions. Our KRIT1 genetic testing provides the clarity and confidence needed for informed medical planning and family health management. With our limited-time discount pricing, now is the perfect opportunity to invest in your genetic health.

Ready to schedule your genetic test? Contact our genetic specialists today:

Phone: +1(267) 388-9828
WhatsApp: +1(267) 388-9828
Booking: Available for immediate scheduling at all locations

Our team of genetic counselors and medical professionals is ready to guide you through the testing process, answer your questions, and provide the comprehensive support you deserve for your genetic health journey.