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MYH8 Gene Arthrogryposis Distal Type 7 Genetic Test

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

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The MYH8 Gene Arthrogryposis Distal Type 7 NGS Genetic DNA Test is a specialized diagnostic examination that identifies mutations in the MYH8 gene responsible for distal arthrogryposis type 7. This comprehensive genetic analysis utilizes next-generation sequencing technology to detect specific genetic variations that cause congenital joint contractures primarily affecting the hands and feet. The test is particularly valuable for individuals presenting with characteristic symptoms such as limited joint mobility, clenched fists, and foot deformities from birth. At only $500 USD, this advanced genetic testing provides crucial diagnostic information that can guide treatment decisions and genetic counseling. The results help healthcare providers develop targeted management strategies and offer accurate recurrence risk assessment for family planning purposes. With a turnaround time of 3-4 weeks and multiple sample collection options including blood, extracted DNA, or blood spots on FTA cards, this test offers accessible and reliable genetic diagnosis for affected individuals and their families.

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MYH8 Gene Arthrogryposis Distal Type 7 NGS Genetic DNA Test

Comprehensive Genetic Analysis for Joint Contracture Disorders

The MYH8 Gene Arthrogryposis Distal Type 7 NGS Genetic DNA Test represents a cutting-edge diagnostic approach for identifying genetic mutations responsible for distal arthrogryposis type 7, a rare congenital condition characterized by multiple joint contractures. This specialized test employs next-generation sequencing technology to provide comprehensive analysis of the MYH8 gene, which encodes myosin heavy chain 8—a crucial protein involved in muscle development and function.

What This Advanced Genetic Test Detects

This sophisticated diagnostic examination specifically targets mutations in the MYH8 gene that are known to cause distal arthrogryposis type 7. The test analyzes the entire coding region of the MYH8 gene to identify:

  • Point mutations affecting myosin heavy chain 8 function
  • Small insertions and deletions disrupting protein structure
  • Missense mutations altering amino acid sequences
  • Pathogenic variants associated with joint contracture development
  • Genetic changes affecting muscle fiber formation and joint mobility

Who Should Consider This Genetic Test

This comprehensive genetic analysis is recommended for individuals presenting with specific clinical features and family history patterns:

  • Newborns or children with congenital joint contractures affecting hands and feet
  • Individuals with characteristic “clenched fist” deformities from birth
  • Patients exhibiting limited range of motion in multiple joints
  • Those with family history of arthrogryposis or similar movement disorders
  • Individuals with unexplained congenital limb deformities
  • Patients requiring differential diagnosis for multiple congenital contractures
  • Families seeking genetic counseling for recurrence risk assessment

Significant Benefits of Genetic Testing

Undergoing the MYH8 Gene Arthrogryposis Distal Type 7 NGS Genetic DNA Test provides numerous advantages for patients and healthcare providers:

  • Accurate Diagnosis: Provides definitive genetic confirmation of distal arthrogryposis type 7
  • Personalized Treatment Planning: Enables development of targeted therapeutic interventions
  • Genetic Counseling Support: Facilitates informed family planning decisions
  • Early Intervention Opportunities: Allows for timely implementation of physical therapy and orthopedic management
  • Comprehensive Risk Assessment: Provides accurate recurrence risk information for family members
  • Differential Diagnosis: Helps distinguish between various forms of arthrogryposis
  • Research Contribution: Advances understanding of MYH8-related disorders

Understanding Your Genetic Test Results

Following test completion, you will receive a comprehensive report detailing the genetic findings:

  • Positive Result: Indicates the presence of a pathogenic MYH8 mutation, confirming the diagnosis of distal arthrogryposis type 7
  • Negative Result: Suggests that no disease-causing mutations were detected in the MYH8 gene
  • Variant of Uncertain Significance: Identifies genetic changes with unclear clinical implications requiring further evaluation
  • Carrier Status: Determines if individuals carry one copy of a mutated gene without showing symptoms

All results are accompanied by detailed interpretation and recommendations from our genetic specialists. We strongly recommend discussing your results with a qualified genetic counselor or healthcare provider to fully understand the implications for your health and family planning.

Test Pricing and Accessibility

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

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

Nationwide Testing Availability

We proudly offer comprehensive genetic testing services across the United States, with convenient locations 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 of certified collection centers ensures accessible testing for patients nationwide.

Take the Next Step Toward Genetic Clarity

Don’t let uncertainty about genetic conditions affect your quality of life. Our MYH8 Gene Arthrogryposis Distal Type 7 NGS Genetic DNA Test provides the definitive answers you need for informed healthcare decisions. With our advanced NGS technology and expert genetic analysis, you can gain valuable insights into your genetic health.

Call or WhatsApp us today at +1(267) 388-9828 to schedule your genetic test consultation and take control of your genetic health journey.

Our dedicated team of genetic specialists is ready to guide you through the testing process, answer your questions, and provide the comprehensive support you deserve. Book your appointment now and begin your path to genetic clarity and personalized healthcare management.