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MID1 Gene Opitz G Syndrome Genetic Test

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

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The MID1 Gene Opitz G Syndrome NGS Genetic DNA Test is a comprehensive genetic screening that identifies mutations in the MID1 gene responsible for Opitz G syndrome, a rare neurological disorder. This advanced next-generation sequencing test provides precise detection of genetic variants associated with craniofacial abnormalities, developmental delays, and neurological complications. The test costs $500 USD and is essential for individuals with family history of the condition or those presenting with characteristic symptoms. Results are available within 3-4 weeks, offering valuable insights for diagnosis and family planning decisions.

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MID1 Gene Opitz G Syndrome NGS Genetic DNA Test

Comprehensive Genetic Testing for Neurological Disorders

The MID1 Gene Opitz G Syndrome NGS Genetic DNA Test represents a breakthrough in neurological genetic diagnostics, offering precise identification of mutations associated with Opitz G syndrome. This rare X-linked genetic disorder primarily affects males and involves multiple congenital anomalies affecting the midline structures of the body. Our advanced testing methodology provides families and healthcare providers with definitive answers for complex neurological conditions.

What Does This Test Measure?

This comprehensive genetic screening specifically targets the MID1 gene located on the X chromosome, which encodes the midline 1 protein crucial for normal embryonic development. The test utilizes next-generation sequencing technology to detect:

  • Point mutations and small insertions/deletions in the MID1 gene
  • Pathogenic variants associated with Opitz G syndrome
  • Genetic markers linked to craniofacial abnormalities
  • Neurological development-related genetic alterations
  • Inheritance patterns for family planning considerations

Who Should Consider This Test?

This genetic screening is recommended for individuals presenting with symptoms suggestive of Opitz G syndrome or those with family history of the condition. Key indications include:

  • Newborns or children with characteristic craniofacial features including hypertelorism, cleft lip/palate, or laryngotracheal abnormalities
  • Individuals with developmental delays, intellectual disability, or neurological impairments
  • Patients with midline defects such as heart abnormalities, hypospadias, or anal anomalies
  • Family members of individuals diagnosed with Opitz G syndrome
  • Couples with family history seeking preconception genetic counseling
  • Individuals with unexplained neurological symptoms matching the syndrome profile

Benefits of MID1 Gene Testing

Choosing our comprehensive genetic testing offers numerous advantages for patients and families:

  • Accurate Diagnosis: Provides definitive confirmation of Opitz G syndrome, eliminating diagnostic uncertainty
  • Family Planning Guidance: Enables informed reproductive decisions through understanding of inheritance patterns
  • Personalized Management: Facilitates targeted medical interventions and specialized care planning
  • Early Intervention: Allows for prompt implementation of developmental therapies and medical treatments
  • Genetic Counseling: Supports comprehensive family risk assessment and education
  • Research Contribution: Advances scientific understanding of rare neurological disorders

Understanding Your Test Results

Our genetic specialists provide comprehensive interpretation of your results with clear guidance:

  • Positive Result: Indicates the presence of a pathogenic MID1 gene mutation, confirming Opitz G syndrome diagnosis
  • Negative Result: Suggests absence of detectable mutations in the MID1 gene, though clinical correlation remains essential
  • Variant of Uncertain Significance: Identifies genetic changes requiring further clinical evaluation and family studies
  • Carrier Status: For female relatives, determines carrier status and associated reproductive risks

All results include detailed consultation with our genetic counselors to ensure complete understanding and appropriate next steps.

Test Pricing Information

Test Component Price (USD)
Discount Price $500
Regular Price $700

Nationwide Testing Availability

We proudly serve patients across the United States with convenient testing 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 genetic testing facilities ensure consistent, high-quality results regardless of location.

Take the Next Step Toward Genetic Clarity

Don’t let uncertainty about neurological symptoms affect your family’s future. Our MID1 Gene Opitz G Syndrome NGS Genetic DNA Test provides the answers you need for informed healthcare decisions. With rapid turnaround times of 3-4 weeks and comprehensive genetic counseling support, we’re committed to delivering exceptional care and accurate results.

Ready to schedule your test? Contact our genetic specialists today at +1(267) 388-9828 or book your appointment online. Take control of your genetic health journey with confidence and clarity.