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HSPG2 Gene Schwartz-Jampel Syndrome Type 1 Genetic Test

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

-29%

The HSPG2 Gene Schwartz-Jampel Syndrome Type 1 NGS Genetic DNA Test is a cutting-edge diagnostic tool that identifies mutations in the HSPG2 gene responsible for Schwartz-Jampel Syndrome Type 1. This rare inherited disorder affects muscle function, bone development, and overall mobility. Using Next-Generation Sequencing (NGS) technology, this test provides comprehensive analysis of the HSPG2 gene to detect pathogenic variants that cause this autosomal recessive condition. The test is essential for individuals experiencing muscle stiffness, joint contractures, facial abnormalities, or growth delays. With results available in 3-4 weeks, this $500 test offers crucial information for accurate diagnosis, family planning, and personalized treatment strategies. Our genetic counseling services ensure proper interpretation and guidance throughout the testing process.

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HSPG2 Gene Schwartz-Jampel Syndrome Type 1 NGS Genetic DNA Test

Comprehensive Introduction to Schwartz-Jampel Syndrome Genetic Testing

The HSPG2 Gene Schwartz-Jampel Syndrome Type 1 NGS Genetic DNA Test represents a breakthrough in neurological genetic diagnostics, offering precise identification of mutations responsible for this rare inherited disorder. Schwartz-Jampel Syndrome Type 1 is an autosomal recessive condition characterized by progressive muscle stiffness, skeletal abnormalities, and distinctive facial features. This advanced testing methodology provides crucial insights for accurate diagnosis and personalized treatment planning.

What Does This Test Measure and Detect?

This sophisticated genetic test specifically analyzes the HSPG2 gene using Next-Generation Sequencing technology to identify pathogenic variants associated with Schwartz-Jampel Syndrome Type 1. The test detects:

  • Point mutations in the HSPG2 gene coding regions
  • Small insertions and deletions affecting gene function
  • Splice site variants that disrupt normal protein production
  • Pathogenic variants affecting perlecan protein structure and function

Who Should Consider This Genetic Test?

This test is recommended for individuals presenting with symptoms suggestive of Schwartz-Jampel Syndrome Type 1, including:

  • Progressive muscle stiffness and myotonia
  • Joint contractures and limited mobility
  • Distinctive facial features including blepharophimosis and pursed lips
  • Short stature and skeletal abnormalities
  • Family history of similar neuromuscular symptoms
  • Unexplained developmental delays with muscle involvement

Significant Benefits of Genetic Testing

Undergoing the HSPG2 genetic test provides numerous advantages for patients and families:

  • Accurate Diagnosis: Confirms or rules out Schwartz-Jampel Syndrome Type 1 with high precision
  • Family Planning: Enables informed reproductive decisions and carrier testing
  • Personalized Treatment: Guides appropriate management strategies and therapeutic interventions
  • Prognostic Information: Helps predict disease progression and potential complications
  • Genetic Counseling: Provides comprehensive family risk assessment and education

Understanding Your Test Results

Our genetic specialists provide detailed interpretation of your test results:

  • Positive Result: Indicates the presence of pathogenic HSPG2 gene mutations confirming Schwartz-Jampel Syndrome Type 1 diagnosis
  • Negative Result: Suggests absence of detectable mutations, though clinical correlation remains essential
  • Variant of Uncertain Significance: Identifies genetic changes requiring further clinical evaluation
  • Carrier Status: Determines if individuals carry one copy of mutated gene without showing symptoms

Test Pricing and Details

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 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 laboratories ensure consistent, reliable results regardless of your location.

Pre-Test Requirements and Genetic Counseling

Before testing, we recommend:

  • Comprehensive clinical history documentation
  • Genetic counseling session with our certified specialists
  • Development of detailed family pedigree chart
  • Discussion of testing implications and potential outcomes

Take Control of Your Genetic Health Today

Don’t let uncertainty about neuromuscular symptoms affect your quality of life. Our HSPG2 Gene Schwartz-Jampel Syndrome Type 1 NGS Genetic DNA Test provides the clarity you need for proper diagnosis and management. With our discounted price of $500 and comprehensive genetic counseling support, you can make informed decisions about your health and future.

Call or WhatsApp us now at +1(267) 388-9828 to schedule your genetic testing appointment or book online through our secure portal. Our genetic specialists are ready to guide you through every step of the testing process and help you understand your results with compassion and expertise.

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