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ACP5 Gene Spondyloenchondrodysplasia with Immune Dysregulation NGS Genetic DNA Test

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

-29%

The ACP5 Gene Spondyloenchondrodysplasia with Immune Dysregulation NGS Genetic DNA Test is a cutting-edge genetic analysis that identifies mutations in the ACP5 gene responsible for rare inherited disorders affecting bone development, immune function, and skin health. Using Next-Generation Sequencing (NGS) technology, this comprehensive test provides precise detection of genetic variants associated with spondyloenchondrodysplasia, a condition characterized by abnormal spinal and bone growth combined with immune system dysfunction. The test is particularly valuable for individuals presenting with skeletal abnormalities, recurrent infections, autoimmune symptoms, or developmental delays. Results help guide personalized treatment strategies and inform family planning decisions. Available for $500 USD, this advanced genetic screening offers crucial insights for patients and families affected by these complex multi-system disorders.

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ACP5 Gene Spondyloenchondrodysplasia with Immune Dysregulation NGS Genetic DNA Test

Comprehensive Genetic Analysis for Complex Multi-System Disorders

The ACP5 Gene Spondyloenchondrodysplasia with Immune Dysregulation NGS Genetic DNA Test represents a breakthrough in genetic diagnostics for rare inherited conditions affecting multiple body systems. This advanced test specifically targets mutations in the ACP5 (acid phosphatase 5) gene, which plays a critical role in bone metabolism, immune regulation, and cellular function. Spondyloenchondrodysplasia with immune dysregulation is a rare autosomal recessive disorder that manifests through complex interactions between skeletal development and immune system function.

What This Test Measures and Detects

Our comprehensive NGS-based genetic test provides detailed analysis of the ACP5 gene to identify pathogenic variants responsible for:

  • Mutations in the ACP5 gene encoding tartrate-resistant acid phosphatase
  • Genetic variants associated with abnormal bone mineralization and growth
  • Mutations causing immune system dysregulation and autoimmune manifestations
  • Inherited patterns of spondyloenchondrodysplasia development
  • Risk assessment for associated complications including neurological symptoms

The test utilizes state-of-the-art Next-Generation Sequencing technology to examine the entire coding region of the ACP5 gene, ensuring comprehensive coverage and high detection rates for both common and rare genetic variants.

Who Should Consider This Genetic Test

This specialized genetic test is recommended for individuals presenting with:

  • Unexplained skeletal abnormalities including short stature and spinal deformities
  • Recurrent infections or immune system dysfunction without clear cause
  • Family history of spondyloenchondrodysplasia or related bone disorders
  • Autoimmune conditions developing in childhood or adolescence
  • Developmental delays combined with skeletal and immune symptoms
  • Skin manifestations including lupus-like rashes or dermatological abnormalities
  • Neurological symptoms such as spasticity or cognitive impairment

Clinical Benefits of Genetic Testing

Undergoing the ACP5 Gene Spondyloenchondrodysplasia with Immune Dysregulation NGS Genetic DNA Test provides numerous clinical advantages:

  • Accurate Diagnosis: Provides definitive genetic confirmation for complex multi-system disorders
  • Personalized Treatment Planning: Enables targeted therapeutic approaches based on specific genetic findings
  • Family Risk Assessment: Identifies inheritance patterns and assesses risk for other family members
  • Reproductive Planning: Informs family planning decisions and prenatal testing options
  • Early Intervention: Facilitates timely management of skeletal, immune, and neurological complications
  • Comprehensive Care Coordination: Guides multidisciplinary care involving genetics, immunology, and orthopedics

Understanding Your Test Results

Our genetic counseling team provides comprehensive interpretation of your test results:

  • Positive Result: Identifies specific ACP5 gene mutations confirming diagnosis, enabling targeted management strategies
  • Negative Result: Rules out ACP5-related disorders, directing further diagnostic evaluation toward other potential causes
  • Variant of Uncertain Significance: Identifies genetic changes requiring additional family studies or research correlation
  • Carrier Status: Determines if individuals carry one copy of a mutated gene without showing symptoms

All results include detailed clinical correlation and recommendations for follow-up care with appropriate specialists.

Test Pricing and Availability

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

Turnaround Time: 3 to 4 Weeks
Sample Type: Blood
Pre-test Requirements: Clinical history documentation and genetic counseling session to create family pedigree chart

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, San Jose, and many other cities. Our network of certified genetic counselors and medical professionals ensures accessible, high-quality genetic testing services nationwide.

Take the Next Step Toward Genetic Clarity

Don’t let uncertainty about complex genetic conditions delay proper diagnosis and treatment. Our ACP5 Gene Spondyloenchondrodysplasia with Immune Dysregulation NGS Genetic DNA Test provides the comprehensive genetic information needed to guide effective medical management and family planning decisions.

Call or WhatsApp us today at +1(267) 388-9828 to schedule your genetic counseling session and book your test. Our dedicated team is ready to assist you with the testing process, answer your questions, and provide the support you need throughout your genetic testing journey.