Congenital Myopathy Gene Panel Test USA | $900 USD | Comprehensive Genetic Testing for Muscle Disorders
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Congenital Myopathy Gene Panel

Original price was: $1,200.Current price is: $900.

-25%

The Congenital Myopathy Gene Panel is a comprehensive genetic test that analyzes multiple genes associated with inherited muscle disorders. This advanced Next-Generation Sequencing (NGS) test helps identify specific genetic mutations causing congenital myopathies, providing crucial diagnostic information for patients experiencing muscle weakness, developmental delays, or respiratory difficulties. The test examines genes responsible for various myopathy types including nemaline myopathy, centronuclear myopathy, and congenital fiber-type disproportion. Results typically take 4-6 weeks and require a doctor’s prescription. At just $900 USD, this test offers valuable insights for treatment planning and genetic counseling, helping families understand inheritance patterns and make informed healthcare decisions.

Clinically Validated & Lab Certified

  • ISO-Accredited Laboratory, Ensuring Highest Standards
  • Trusted by Hospitals & Patients —Accredited Testing with Results
  • Direct Healthcare Provider Support + Comprehensive Reporting
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Congenital Myopathy Gene Panel: Comprehensive Genetic Testing for Inherited Muscle Disorders

Understanding Congenital Myopathy Genetic Testing

Congenital myopathies represent a group of rare genetic muscle disorders that typically present at birth or during early childhood. These conditions affect muscle structure and function, leading to progressive muscle weakness, respiratory complications, and developmental challenges. The Congenital Myopathy Gene Panel utilizes cutting-edge Next-Generation Sequencing (NGS) technology to analyze multiple genes simultaneously, providing comprehensive genetic insights into these complex disorders.

What This Advanced Genetic Test Detects

Our comprehensive panel examines over 50 genes associated with various forms of congenital myopathy, including:

  • Nemaline myopathy genes (NEB, ACTA1, TPM2, TPM3)
  • Centronuclear myopathy genes (MTM1, DNM2, BIN1)
  • Congenital fiber-type disproportion genes (TPM3, ACTA1, SEPN1)
  • Core myopathy genes (RYR1, SEPN1)
  • Other myopathy-associated genetic markers

Who Should Consider Congenital Myopathy Genetic Testing?

This test is particularly valuable for individuals experiencing:

  • Infants and children with unexplained muscle weakness
  • Delayed motor milestones and developmental concerns
  • Respiratory difficulties requiring ventilator support
  • Family history of inherited muscle disorders
  • Abnormal muscle biopsy findings
  • Feeding difficulties and failure to thrive in infancy
  • Skeletal abnormalities and joint contractures

Clinical Benefits of Genetic Testing

Undergoing the Congenital Myopathy Gene Panel provides numerous advantages:

  • Accurate Diagnosis: Precise identification of specific genetic mutations
  • Personalized Treatment: Targeted therapeutic approaches based on genetic findings
  • Family Planning: Understanding inheritance patterns for future generations
  • Prognostic Information: Better understanding of disease progression and outcomes
  • Research Opportunities: Potential eligibility for clinical trials and emerging treatments

Understanding Your Test Results

Our comprehensive genetic analysis provides detailed insights into your condition:

  • Positive Results: Identification of pathogenic variants confirms diagnosis and guides management
  • Negative Results: No detected mutations may suggest alternative diagnoses
  • Variant of Uncertain Significance: Genetic changes requiring further clinical correlation
  • Carrier Status: Information about inheritance risks for family members

Test Pricing and Availability

Test Component Price (USD)
Discount Price $900
Regular Price $1200

Test Specifications

  • Turnaround Time: 4-6 weeks
  • Sample Type: Amniotic fluid, Chorionic villi, or Peripheral blood
  • Test Components: Sterile container, Sterile Normal Saline Container, EDTA Vacutainer
  • Methodology: Next-Generation Sequencing (NGS)

Nationwide Testing Availability

We have diagnostic centers conveniently located across the United States, serving patients in major metropolitan areas including New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, and many other cities. Our state-of-the-art laboratories ensure consistent, high-quality testing regardless of location.

Pre-Test Requirements

The Congenital Myopathy Gene Panel requires a physician’s prescription for testing. Please note that prescriptions are not applicable for surgical cases, pregnancy-related testing, or individuals planning international travel. Consult with your healthcare provider to determine if this test is appropriate for your specific situation.

Take Control of Your Genetic Health Today

Don’t let uncertainty about muscle weakness or developmental concerns continue. Our comprehensive Congenital Myopathy Gene Panel provides the answers you need for informed medical decisions and personalized care planning. With advanced NGS technology and expert genetic analysis, we deliver reliable results that can transform your healthcare journey.

Ready to begin your genetic testing journey? Call our dedicated genetic counseling team at +1(267) 388-9828 or book your appointment online today. Take the first step toward understanding your genetic health and accessing targeted treatment options.

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