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LPIN2 Gene Majeed Syndrome NGS Genetic DNA Test

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

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The LPIN2 Gene Majeed Syndrome NGS Genetic DNA Test is a comprehensive genetic analysis that identifies mutations in the LPIN2 gene responsible for Majeed syndrome. This rare autosomal recessive disorder affects multiple body systems, primarily causing chronic recurrent multifocal osteomyelitis, congenital dyserythropoietic anemia, and inflammatory dermatosis. Using next-generation sequencing technology, this test provides precise detection of pathogenic variants to confirm diagnosis, guide treatment decisions, and facilitate genetic counseling. The test is particularly valuable for individuals with recurrent bone inflammation, unexplained anemia, and persistent skin conditions. At only $500 USD, this advanced genetic testing offers crucial insights for managing this complex multisystem disorder and understanding inheritance patterns within families.

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LPIN2 Gene Majeed Syndrome NGS Genetic DNA Test

Comprehensive Genetic Analysis for Majeed Syndrome

The LPIN2 Gene Majeed Syndrome NGS Genetic DNA Test represents a cutting-edge diagnostic approach for identifying mutations in the LPIN2 gene, which are responsible for Majeed syndrome. This rare autosomal recessive disorder presents as a complex multisystem condition affecting bone development, blood cell production, and skin integrity. Our advanced next-generation sequencing technology provides unparalleled accuracy in detecting pathogenic variants, enabling precise diagnosis and informed clinical management decisions.

What This Test Measures and Detects

This comprehensive genetic test specifically analyzes the LPIN2 gene using next-generation sequencing technology to identify:

  • Pathogenic mutations in the LPIN2 gene associated with Majeed syndrome
  • Single nucleotide variants, insertions, deletions, and copy number variations
  • Autosomal recessive inheritance patterns
  • Specific genetic markers linked to chronic recurrent multifocal osteomyelitis
  • Variants associated with congenital dyserythropoietic anemia
  • Genetic factors contributing to inflammatory dermatosis

Who Should Consider This Test

This genetic test is recommended for individuals presenting with the following symptoms or clinical indications:

  • Recurrent episodes of bone pain and inflammation without clear infectious cause
  • Unexplained anemia that doesn’t respond to conventional treatments
  • Persistent inflammatory skin conditions beginning in early childhood
  • Family history of similar multisystem inflammatory disorders
  • Children with recurrent fever episodes and bone abnormalities
  • Patients with suspected autoinflammatory bone diseases
  • Individuals with consanguineous parents or family history of genetic disorders

Clinical Benefits of Genetic Testing

Undergoing the LPIN2 Gene Majeed Syndrome NGS Genetic DNA Test provides numerous clinical advantages:

  • Accurate Diagnosis: Confirms or rules out Majeed syndrome with high precision
  • Personalized Treatment: Enables targeted therapeutic approaches based on genetic findings
  • Family Planning: Provides crucial information for genetic counseling and reproductive decisions
  • Early Intervention: Facilitates prompt management to prevent disease complications
  • Differential Diagnosis: Helps distinguish Majeed syndrome from other autoinflammatory conditions
  • Prognostic Information: Offers insights into disease progression and potential outcomes

Understanding Your Test Results

Our comprehensive genetic report provides clear interpretation of your results with the following possible outcomes:

  • Positive Result: Identifies pathogenic mutations in the LPIN2 gene, confirming Majeed syndrome diagnosis and enabling targeted management strategies
  • Negative Result: No pathogenic variants detected, suggesting alternative diagnoses should be considered
  • Variant of Uncertain Significance: Identifies genetic changes with unclear clinical implications, requiring further evaluation and possibly family studies
  • Carrier Status: Identifies individuals with one mutated copy who may pass the condition to offspring if their partner is also a carrier

Test Specifications and Pricing

Test Component Details
Test Name LPIN2 Gene Majeed Syndrome 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
Specialty Dermatology, Genetics, Osteology, Immunology

Pre-Test Requirements

To ensure optimal testing outcomes, please provide:

  • Complete clinical history of the patient undergoing testing
  • Genetic counseling session to create a detailed pedigree chart of family members affected by LPIN2 gene-related conditions
  • Documentation of current symptoms and previous diagnostic evaluations
  • Informed consent for genetic testing and result disclosure

Nationwide Accessibility

We have diagnostic centers conveniently located across the United States, including major metropolitan areas such as New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, San Jose, and many other cities. Our network ensures accessible genetic testing services for patients throughout the country.

Take the Next Step Toward Genetic Clarity

Don’t let uncertainty about your genetic health prevent you from getting the answers you need. Our LPIN2 Gene Majeed Syndrome NGS Genetic DNA Test provides the comprehensive analysis required for accurate diagnosis and informed medical decisions. With our discounted price of only $500 USD and rapid 3-4 week turnaround time, 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 health journey.

Our experienced genetic counselors and medical professionals are ready to guide you through the testing process, answer your questions, and provide the support you need throughout your diagnostic journey. Book your appointment now and move forward with confidence in your genetic health management.