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IDUA Gene Mucopolysaccharidosis Type 1H Genetic Test

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

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The IDUA Gene Mucopolysaccharidosis Type 1H NGS Genetic DNA Test is a comprehensive genetic screening that detects mutations in the IDUA gene responsible for Hurler Syndrome, a severe form of mucopolysaccharidosis. This advanced next-generation sequencing test provides precise identification of genetic variants that cause enzyme deficiencies leading to progressive cellular damage. Early detection through this $500 USD test enables timely intervention, personalized treatment planning, and informed family counseling. The test is particularly crucial for individuals showing developmental delays, skeletal abnormalities, or family history of metabolic disorders. Results are delivered within 3-4 weeks, offering valuable insights for managing this rare inherited condition.

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IDUA Gene Mucopolysaccharidosis Type 1H NGS Genetic DNA Test

Comprehensive Genetic Testing for Hurler Syndrome

The IDUA Gene Mucopolysaccharidosis Type 1H NGS Genetic DNA Test represents a breakthrough in genetic diagnostics for Hurler Syndrome, a severe inherited metabolic disorder. This advanced testing methodology utilizes next-generation sequencing technology to provide unparalleled accuracy in detecting mutations within the IDUA gene, which encodes the alpha-L-iduronidase enzyme essential for proper cellular function.

What This Test Measures and Detects

This sophisticated genetic analysis specifically targets the IDUA gene located on chromosome 4p16.3, examining it for pathogenic variants that disrupt normal enzyme production. The test identifies:

  • Point mutations, deletions, and insertions within the IDUA gene
  • Specific genetic variants associated with alpha-L-iduronidase deficiency
  • Mutations responsible for impaired glycosaminoglycan metabolism
  • Genetic markers indicating Hurler Syndrome susceptibility
  • Inheritance patterns for family planning considerations

Who Should Consider This Genetic Test

This comprehensive genetic screening is recommended for individuals presenting with:

  • Progressive developmental delays in infancy or early childhood
  • Characteristic coarse facial features and skeletal abnormalities
  • Recurrent respiratory infections and breathing difficulties
  • Hearing loss and vision problems including corneal clouding
  • Organ enlargement, particularly hepatosplenomegaly
  • Family history of mucopolysaccharidosis or unexplained infant deaths
  • Unexplained cardiac complications in young children
  • Suspected metabolic storage disorders based on clinical presentation

Clinical Benefits of Early Genetic Detection

Early identification through this genetic test provides numerous clinical advantages:

  • Enables timely initiation of enzyme replacement therapy
  • Facilitates early consideration of hematopoietic stem cell transplantation
  • Provides accurate genetic counseling for family planning decisions
  • Allows for proactive management of potential complications
  • Supports personalized treatment strategies based on specific mutation types
  • Reduces diagnostic uncertainty and enables targeted interventions

Understanding Your Test Results

Your genetic test report will provide comprehensive information about your IDUA gene status:

  • Normal Result: No pathogenic variants detected in the IDUA gene
  • Carrier Status: Identification of one mutated copy with one normal copy
  • Affected Status: Detection of two pathogenic mutations confirming diagnosis
  • Variant of Uncertain Significance: Genetic changes requiring further clinical correlation

All positive results include detailed interpretation by certified genetic counselors to ensure proper understanding and appropriate next steps.

Test Pricing and Availability

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 Accessibility

We maintain comprehensive testing facilities across the United States, with specialized genetic testing centers in all major metropolitan areas including New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, and San Jose. Our network ensures convenient access to advanced genetic diagnostics regardless of your location.

Pre-Test Requirements and Preparation

To ensure optimal testing accuracy, we recommend:

  • Complete clinical history documentation for the patient
  • Genetic counseling session to create detailed family pedigree
  • Discussion of testing implications with healthcare providers
  • Understanding of potential outcomes and their significance

Take Control of Your Genetic Health Today

Don’t let uncertainty about genetic conditions affect your family’s future. Our IDUA Gene Mucopolysaccharidosis Type 1H NGS Genetic DNA Test provides the clarity needed for informed healthcare decisions. With our discounted price of $500 and comprehensive nationwide coverage, advanced genetic testing has never been more accessible.

Call or WhatsApp us today at +1(267) 388-9828 to schedule your genetic test consultation and take the first step toward genetic clarity and personalized healthcare planning.