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NAA10 Gene Ogden Syndrome NGS Genetic DNA Test

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

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The NAA10 Gene Ogden Syndrome NGS Genetic DNA Test is a comprehensive genetic analysis that identifies mutations in the NAA10 gene associated with Ogden syndrome. This rare genetic disorder is characterized by developmental delays, intellectual disability, distinctive facial features, and cardiac abnormalities. Using Next-Generation Sequencing (NGS) technology, this test provides precise detection of genetic variants that cause this condition. The test is essential for individuals showing symptoms of developmental disorders, unexplained intellectual disabilities, or dysmorphic features. Early diagnosis through this test enables proper medical management, genetic counseling, and family planning. Available for $500 USD, this advanced genetic testing offers crucial insights for affected individuals and their families.

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NAA10 Gene Ogden Syndrome NGS Genetic DNA Test

Comprehensive Genetic Testing for Developmental Disorders

The NAA10 Gene Ogden Syndrome NGS Genetic DNA Test represents a cutting-edge approach to diagnosing rare genetic conditions affecting neurological development and physical growth. This specialized test utilizes advanced Next-Generation Sequencing technology to analyze the NAA10 gene, which plays a critical role in protein acetylation and cellular function regulation.

What is Ogden Syndrome?

Ogden syndrome is an extremely rare X-linked genetic disorder caused by mutations in the NAA10 gene. This condition primarily affects males and is characterized by a distinctive combination of developmental delays, intellectual disability, characteristic facial features, and cardiac abnormalities. The NAA10 gene encodes an enzyme involved in N-terminal acetylation, a crucial protein modification process essential for proper cellular function and development.

What the Test Measures and Detects

This comprehensive genetic test specifically targets:

  • Complete sequencing of the NAA10 gene using NGS technology
  • Detection of point mutations, insertions, and deletions
  • Identification of pathogenic variants associated with Ogden syndrome
  • Analysis of genetic changes affecting protein function
  • Assessment of variant pathogenicity and clinical significance

Who Should Consider This Test?

Clinical Indications and Symptoms

This test is recommended for individuals presenting with:

  • Unexplained developmental delays in infancy or childhood
  • Intellectual disability of unknown origin
  • Distinctive facial features including prominent forehead, deep-set eyes, and full cheeks
  • Cardiac abnormalities or arrhythmias
  • Growth retardation and failure to thrive
  • Family history of similar symptoms or known NAA10 mutations
  • Unexplained neurological symptoms in male infants

Benefits of NAA10 Genetic Testing

Comprehensive Diagnostic Advantages

  • Accurate Diagnosis: Provides definitive genetic confirmation of Ogden syndrome
  • Early Intervention: Enables timely medical management and therapeutic interventions
  • Family Planning: Offers crucial information for genetic counseling and reproductive decisions
  • Personalized Care: Guides targeted treatment approaches based on genetic findings
  • Prognostic Information: Helps understand disease progression and potential complications
  • Research Contribution: Contributes to scientific understanding of rare genetic disorders

Understanding Your Test Results

Interpreting Genetic Findings

Your test results will be carefully analyzed and interpreted by our team of genetic specialists:

  • Positive Result: Indicates the presence of a pathogenic NAA10 mutation consistent with Ogden syndrome diagnosis
  • Negative Result: Suggests no disease-causing mutations were detected in the NAA10 gene
  • Variant of Uncertain Significance: Identifies genetic changes whose clinical significance requires further investigation
  • Carrier Status: For female relatives, indicates carrier status and inheritance risk

All results include comprehensive genetic counseling to ensure proper understanding and appropriate next steps for medical management.

Test Details and Pricing

Test Information Details
Test Name NAA10 Gene Ogden 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

Pre-Test Requirements

Essential Preparation Steps

  • Complete clinical history documentation of the patient
  • Genetic counseling session to create detailed family pedigree
  • Identification of affected family members with similar symptoms
  • Discussion of testing implications and potential outcomes
  • Informed consent process for genetic testing

Nationwide Testing Availability

We have conveniently located branches across the United States, serving patients 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 genetic testing facilities ensures accessible, high-quality care for patients nationwide.

Take the Next Step Toward Genetic Clarity

If you or your loved one is experiencing symptoms suggestive of Ogden syndrome or related developmental disorders, don’t wait to get answers. Our comprehensive NAA10 genetic testing provides the clarity needed for proper diagnosis and management.

Call or WhatsApp us today at +1(267) 388-9828 to schedule your genetic counseling session and book your NAA10 Gene Ogden Syndrome NGS Genetic DNA Test. Our dedicated genetic specialists are ready to guide you through the testing process and help you understand your results.

Early genetic diagnosis can make a significant difference in managing developmental disorders and planning appropriate interventions. Trust our expertise in genetic testing to provide the answers you need for better health outcomes.