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MED12 Gene FG Syndrome Type 1 Genetic Test

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

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The MED12 Gene FG Syndrome Type 1 NGS Genetic DNA Test is a comprehensive genetic screening that identifies mutations in the MED12 gene associated with FG syndrome type 1, a rare X-linked neurological disorder. This advanced next-generation sequencing test provides crucial insights for individuals experiencing developmental delays, intellectual disabilities, or congenital anomalies. The test helps confirm diagnosis, guide treatment strategies, and inform family planning decisions. With results available in 3-4 weeks and requiring only a blood sample or DNA extraction, this $500 USD test offers accessible genetic testing across our nationwide network of facilities. Our experienced genetic counselors provide pre-test counseling and comprehensive result interpretation to ensure you receive the most accurate and actionable genetic information.

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MED12 Gene FG Syndrome Type 1 NGS Genetic DNA Test

Comprehensive Genetic Testing for Neurological Disorders

The MED12 Gene FG Syndrome Type 1 NGS Genetic DNA Test represents a cutting-edge approach to diagnosing rare neurological conditions through advanced genetic analysis. This specialized test focuses on identifying mutations in the MED12 gene, which plays a critical role in neurological development and function. FG syndrome type 1 is an X-linked genetic disorder characterized by distinctive physical features, intellectual disability, and developmental challenges that can significantly impact quality of life.

What Does This Test Measure?

This comprehensive genetic analysis utilizes Next-Generation Sequencing (NGS) technology to examine the MED12 gene for specific mutations associated with FG syndrome type 1. The test detects:

  • Point mutations in the MED12 gene coding regions
  • Small insertions and deletions affecting gene function
  • Genetic variants that disrupt normal neurological development
  • X-linked inheritance patterns specific to FG syndrome

Who Should Consider This Test?

This genetic test is particularly important for individuals presenting with symptoms suggestive of FG syndrome type 1, including:

  • Children with developmental delays and intellectual disabilities
  • Individuals with congenital anomalies affecting multiple body systems
  • Patients with characteristic facial features associated with FG syndrome
  • Family members of individuals diagnosed with MED12-related disorders
  • Those with unexplained neurological symptoms and family history of similar conditions

Key Benefits of MED12 Genetic Testing

Undergoing MED12 gene testing provides numerous advantages for patients and families:

  • Accurate Diagnosis: Confirms or rules out FG syndrome type 1 with high precision
  • Personalized Care: Enables targeted treatment and management strategies
  • Family Planning: Provides crucial information for genetic counseling and reproductive decisions
  • Early Intervention: Facilitates timely support services and educational planning
  • Peace of Mind: Reduces diagnostic uncertainty and provides clear answers

Understanding Your Test Results

Our comprehensive result interpretation includes:

  • Positive Result: Indicates the presence of a MED12 gene mutation associated with FG syndrome type 1, requiring follow-up with a neurologist and genetic counselor
  • Negative Result: Suggests no detectable MED12 mutation, though other genetic causes may need investigation
  • Variant of Uncertain Significance: Identifies genetic changes with unclear clinical implications, requiring ongoing monitoring

All results are accompanied by detailed explanations and recommendations from our certified genetic counselors to ensure you fully understand the implications for your health and family.

Test Pricing and Sample Requirements

Test Name Discount Price Regular Price
MED12 Gene FG Syndrome Type 1 NGS Genetic DNA Test $500 USD $700 USD

Turnaround Time: 3 to 4 Weeks
Sample Type: Blood, Extracted DNA, or One Drop Blood on FTA Card

Pre-Test Preparation

Before undergoing testing, we recommend:

  • Comprehensive clinical history documentation
  • Genetic counseling session with our specialists
  • Development of a detailed family pedigree chart
  • Discussion of potential outcomes and implications

Nationwide Testing Availability

We have conveniently located branches across the United States, serving 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 facilities ensure consistent, high-quality testing standards nationwide.

Book Your Test Today

Take the first step toward understanding your genetic health. Our experienced team of neurologists and genetic specialists is ready to provide comprehensive care and support throughout your testing journey.

Call or WhatsApp us today at +1(267) 388-9828 to schedule your appointment or learn more about the MED12 Gene FG Syndrome Type 1 NGS Genetic DNA Test. Our genetic counselors are available to answer your questions and guide you through the testing process.