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MED13L Gene Mental Retardation and Distinctive Facial Features with or without Cardiac Defects NGS Genetic DNA Test

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

-29%

The MED13L Gene NGS Genetic DNA Test is a comprehensive diagnostic tool that identifies mutations in the MED13L gene associated with intellectual disability, distinctive facial characteristics, and potential cardiac abnormalities. This advanced next-generation sequencing test provides precise detection of genetic variants responsible for MED13L-related neurodevelopmental disorders. The test is crucial for individuals presenting with developmental delays, cognitive impairment, unique facial features, or congenital heart defects. By offering definitive genetic diagnosis, this test enables proper medical management, genetic counseling, and family planning decisions. Our specialized genetic testing service is available at $500 USD with comprehensive pre-test genetic counseling included.

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  • ISO-Accredited Laboratory, Ensuring Highest Standards
  • Trusted by Hospitals & Patients —Accredited Testing with Results
  • Direct Healthcare Provider Support + Comprehensive Reporting
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MED13L Gene Mental Retardation and Distinctive Facial Features with or without Cardiac Defects NGS Genetic DNA Test

Comprehensive Genetic Testing for MED13L-Related Disorders

The MED13L Gene NGS Genetic DNA Test represents a cutting-edge diagnostic approach for identifying mutations in the MED13L gene, which plays a critical role in neurological development and cardiac formation. This specialized genetic test utilizes next-generation sequencing technology to provide comprehensive analysis of the MED13L gene, enabling accurate diagnosis of MED13L-related neurodevelopmental disorders characterized by intellectual disability, distinctive facial features, and potential cardiac abnormalities.

What Does the MED13L Gene Test Detect?

Our advanced NGS-based MED13L genetic test specifically identifies:

  • Pathogenic variants and mutations in the MED13L gene
  • Single nucleotide variants (SNVs) affecting gene function
  • Small insertions and deletions (indels) within the gene sequence
  • Copy number variations impacting MED13L gene dosage
  • Regulatory region mutations affecting gene expression

Who Should Consider MED13L Genetic Testing?

This comprehensive genetic test is recommended for individuals presenting with:

Clinical Indications and Symptoms

  • Developmental delay and intellectual disability of unknown cause
  • Distinctive facial features including prominent forehead, deep-set eyes, and thin upper lip
  • Congenital heart defects or cardiac abnormalities
  • Speech and language development delays
  • Motor coordination difficulties and hypotonia
  • Behavioral challenges including autism spectrum features
  • Family history of similar neurodevelopmental conditions
  • Unexplained seizures or neurological symptoms

Benefits of MED13L Genetic DNA Testing

Comprehensive Diagnostic Advantages

  • Definitive Diagnosis: Provides clear genetic confirmation of MED13L-related disorders
  • Personalized Management: Enables targeted medical care and intervention strategies
  • Family Planning Guidance: Offers crucial information for reproductive decision-making
  • Early Intervention: Facilitates timely therapeutic approaches for better outcomes
  • Genetic Counseling: Supports comprehensive family risk assessment and education
  • Research Contribution: Advances understanding of MED13L-related conditions

Understanding Your MED13L Test Results

Interpretation and Clinical Implications

Our comprehensive genetic counseling service ensures proper understanding of your test results:

  • Positive Result: Indicates presence of pathogenic MED13L mutation, confirming diagnosis and guiding management
  • Negative Result: Suggests MED13L mutation is unlikely the cause of symptoms, prompting further evaluation
  • Variant of Uncertain Significance: Requires additional family studies and ongoing research correlation
  • Carrier Status: Identifies individuals with single copy mutations who may pass condition to offspring

MED13L Gene Test Pricing and Details

Test Component Details
Test Name MED13L Gene Mental Retardation and Distinctive Facial Features with or without Cardiac Defects 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 Pediatrics and Genetics

Nationwide Testing Availability

We provide comprehensive MED13L genetic testing services across the United States with convenient locations in major cities including New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, and San Jose. Our network of certified genetic counselors and medical professionals ensures accessible, high-quality genetic testing services nationwide.

Pre-Test Requirements and Genetic Counseling

Before undergoing MED13L genetic testing, we require:

  • Complete clinical history of the patient
  • Comprehensive genetic counseling session
  • Detailed pedigree chart documenting family members affected with similar conditions
  • Informed consent for genetic testing
  • Discussion of potential outcomes and implications

Take the Next Step Toward Genetic Clarity

Don’t let uncertainty about genetic conditions affect your family’s future. Our MED13L Gene NGS Genetic DNA Test provides the answers you need for informed medical decisions and comprehensive care planning. With our advanced testing technology and expert genetic counseling team, you can achieve definitive diagnosis and personalized management strategies.

Book your MED13L genetic test today or call our genetic specialists at +1(267) 388-9828 to schedule your comprehensive genetic counseling session and testing appointment.