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DMD Gene Muscular Dystrophy Becker Type Genetic Test

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

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The DMD Gene Muscular Dystrophy Becker Type NGS Genetic DNA Test is a comprehensive genetic analysis that detects mutations in the DMD gene responsible for Becker muscular dystrophy. This advanced next-generation sequencing test provides precise identification of genetic variants that cause this progressive muscle-wasting disorder. The test is essential for individuals experiencing muscle weakness, delayed motor milestones, or with family history of muscular dystrophy. Results help guide treatment decisions, inform family planning, and enable early intervention strategies. Available for only $500 USD, this test offers crucial diagnostic information for patients and healthcare providers managing neurological disorders.

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DMD Gene Muscular Dystrophy Becker Type NGS Genetic DNA Test

Comprehensive Genetic Testing for Becker Muscular Dystrophy

The DMD Gene Muscular Dystrophy Becker Type NGS Genetic DNA Test represents a breakthrough in genetic diagnostics for neuromuscular disorders. This advanced testing methodology utilizes next-generation sequencing technology to provide comprehensive analysis of the DMD gene, which plays a critical role in muscle function and integrity. Becker muscular dystrophy is an X-linked recessive disorder characterized by progressive muscle weakness and wasting, typically presenting in childhood or adolescence with a slower progression compared to Duchenne muscular dystrophy.

What This Test Measures and Detects

This sophisticated genetic test specifically targets the DMD gene located on the X chromosome, analyzing for various types of mutations including:

  • Deletions and duplications in the dystrophin gene
  • Point mutations affecting protein function
  • Frameshift mutations disrupting gene reading
  • Splice site variants affecting RNA processing
  • Complex rearrangements within the gene structure

The test provides comprehensive coverage of all 79 exons of the DMD gene, ensuring no potential mutation goes undetected. By identifying the specific genetic alteration responsible for Becker muscular dystrophy, healthcare providers can offer more targeted treatment approaches and accurate prognosis predictions.

Who Should Consider This Genetic Test

This test is recommended for individuals presenting with specific clinical symptoms or risk factors:

  • Males experiencing progressive muscle weakness, particularly in pelvic and shoulder girdles
  • Individuals with elevated creatine kinase levels without clear explanation
  • Patients with delayed motor milestones or difficulty with physical activities
  • Those with family history of muscular dystrophy or unexplained muscle disorders
  • Individuals experiencing muscle cramps, stiffness, or pseudohypertrophy
  • Patients with cardiac involvement or respiratory complications of unknown origin
  • Family members of confirmed Becker muscular dystrophy cases for carrier testing

Significant Benefits of Genetic Testing

Undergoing the DMD Gene Muscular Dystrophy Becker Type NGS Genetic DNA Test offers numerous advantages:

  • Accurate Diagnosis: Provides definitive genetic confirmation of Becker muscular dystrophy, eliminating diagnostic uncertainty
  • Personalized Treatment Planning: Enables healthcare providers to develop targeted management strategies based on specific mutation type
  • Family Planning Guidance: Offers crucial information for genetic counseling and reproductive decision-making
  • Early Intervention Opportunities: Facilitates proactive management of potential complications before they become severe
  • Clinical Trial Eligibility: May qualify patients for emerging therapies and research studies
  • Psychological Relief: Provides clarity and reduces anxiety associated with undiagnosed symptoms

Understanding Your Test Results

Our comprehensive genetic testing provides detailed insights into your DMD gene status:

  • Positive Result: Indicates the presence of a pathogenic mutation in the DMD gene consistent with Becker muscular dystrophy diagnosis
  • Negative Result: Suggests no detectable mutations in the DMD gene, though clinical correlation remains essential
  • Variant of Uncertain Significance: Identifies genetic changes whose clinical significance requires further investigation
  • Carrier Status: For female relatives, determines whether they carry the mutation and risk passing it to offspring

All results include detailed interpretation by our board-certified genetic specialists, with recommendations for next steps and management considerations. Genetic counseling is strongly recommended to fully understand the implications of your results.

Test Information and Pricing

Test Component Details
Test Name DMD Gene Muscular Dystrophy Becker Type NGS Genetic DNA Test
Regular Price $700 USD
Discount Price $500 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

Nationwide Accessibility and Convenience

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, San Jose, and many more. Our network of certified collection centers ensures easy access to this crucial genetic testing regardless of your location.

Take Control of Your Health Today

Don’t let uncertainty about muscle weakness or family history of muscular dystrophy continue to cause concern. The DMD Gene Muscular Dystrophy Becker Type NGS Genetic DNA Test provides the clarity and answers you need to make informed healthcare decisions. Our team of genetic specialists and neurologists are ready to support you through every step of the testing process.

Call or WhatsApp us today at +1(267) 388-9828 to schedule your genetic testing appointment or to speak with our genetic counseling team. Take the first step toward understanding your genetic health and securing your future wellbeing.