Sale!

MID2 Gene Mental Retardation X-Linked Type 101 Genetic Test

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

-29%

The MID2 Gene Mental Retardation X-Linked Type 101 NGS Genetic DNA Test is a comprehensive genetic analysis that identifies mutations in the MID2 gene responsible for X-linked intellectual disability. This advanced next-generation sequencing test provides crucial diagnostic information for individuals experiencing developmental delays, cognitive impairments, and neurological symptoms. The test helps confirm genetic causes of intellectual disability, enables accurate family planning decisions, and provides essential information for clinical management. At only $500 USD, this test offers accessible genetic testing using state-of-the-art NGS technology with results available in 3-4 weeks. Our testing process includes genetic counseling and supports families in understanding inherited neurological conditions.

Trusted Testing. Expert Care. Guaranteed Privacy.

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

MID2 Gene Mental Retardation X-Linked Type 101 NGS Genetic DNA Test

Comprehensive Genetic Testing for X-Linked Intellectual Disability

The MID2 Gene Mental Retardation X-Linked Type 101 NGS Genetic DNA Test represents a breakthrough in genetic diagnostics for neurological disorders. This specialized test utilizes cutting-edge Next-Generation Sequencing (NGS) technology to identify mutations in the MID2 gene, which plays a crucial role in brain development and cognitive function. Understanding the genetic basis of intellectual disability is essential for accurate diagnosis, appropriate medical management, and informed family planning decisions.

What Does This Test Measure?

This comprehensive genetic analysis specifically targets the MID2 gene located on the X chromosome, which is associated with X-linked intellectual disability type 101. The test detects:

  • Point mutations and small insertions/deletions in the MID2 gene
  • Genetic variants that disrupt normal brain development
  • X-linked inheritance patterns affecting male family members
  • Specific mutations known to cause intellectual disability and developmental delays

Who Should Consider This Test?

This genetic test is recommended for individuals displaying symptoms of intellectual disability or developmental delays, particularly when there is a family history suggesting X-linked inheritance. Consider testing if you or your family members experience:

  • Significant developmental delays in childhood
  • Intellectual disability ranging from mild to severe
  • Learning difficulties and cognitive impairments
  • Speech and language development delays
  • Motor skill development challenges
  • Family history of intellectual disability affecting primarily males
  • Unexplained neurological symptoms in multiple male relatives

Key Benefits of MID2 Genetic Testing

Undergoing the MID2 Gene Mental Retardation X-Linked Type 101 NGS Genetic DNA Test provides numerous advantages for patients and families:

  • Accurate Diagnosis: Confirms or rules out MID2-related intellectual disability with high precision
  • Family Planning Guidance: Provides essential information for genetic counseling and reproductive decisions
  • Personalized Management: Enables targeted interventions and educational support strategies
  • Early Intervention: Facilitates timely therapeutic approaches for better outcomes
  • Genetic Counseling Support: Includes pre-test counseling to understand inheritance patterns
  • Comprehensive Analysis: Utilizes advanced NGS technology for thorough genetic assessment

Understanding Your Test Results

Your genetic test results will be thoroughly explained by our genetic counseling team. Possible outcomes include:

  • Positive Result: Indicates the presence of a pathogenic MID2 gene mutation confirming the diagnosis of X-linked intellectual disability type 101
  • Negative Result: Suggests that MID2 gene mutations are not the cause of symptoms, though other genetic factors may be involved
  • Variant of Uncertain Significance: Identifies a genetic change whose clinical significance requires further investigation
  • Carrier Status: For female relatives, identifies carrier status which has implications for family planning

Test Details and Pricing

Test Component Details
Test Name MID2 Gene Mental Retardation X-Linked Type 101 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
Specialty Neurology & Genetics

Pre-Test Requirements

Before undergoing testing, we require:

  • Complete clinical history of the patient
  • Genetic counseling session to discuss testing implications
  • Development of a detailed family pedigree chart
  • Informed consent understanding the test limitations and benefits

Nationwide Accessibility

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 more. Our network ensures accessible genetic testing services regardless of your location.

Take the Next Step Toward Genetic Clarity

Don’t let uncertainty about genetic causes of intellectual disability affect your family’s future. Our MID2 Gene Mental Retardation X-Linked Type 101 NGS Genetic DNA Test provides the answers you need for informed medical decisions and family planning. With our discounted price of $500 USD and comprehensive genetic counseling support, you can access world-class genetic testing with confidence.

Call us today at +1(267) 388-9828 to schedule your genetic counseling session and book your test. Our genetic specialists are ready to guide you through the testing process and help you understand your results.

Take control of your genetic health with advanced NGS technology and expert medical guidance. Contact us now to begin your journey toward genetic clarity and personalized medical management.