LAS1L Gene Wilson-Turner Syndrome NGS Genetic DNA Test
Comprehensive Genetic Testing for Wilson-Turner Syndrome
The LAS1L Gene Wilson-Turner Syndrome NGS Genetic DNA Test represents a breakthrough in neurological genetic diagnostics, offering precise identification of mutations responsible for this rare inherited condition. Wilson-Turner syndrome is a complex neurological disorder characterized by developmental delays, intellectual disability, and distinctive physical features. Our advanced testing methodology provides families and healthcare providers with definitive genetic information crucial for accurate diagnosis and personalized treatment strategies.
What This Test Measures and Detects
This sophisticated genetic analysis specifically targets the LAS1L gene using next-generation sequencing (NGS) technology to identify pathogenic variants associated with Wilson-Turner syndrome. The test examines:
- Point mutations and single nucleotide variants in the LAS1L gene
- Small insertions and deletions affecting gene function
- Copy number variations and structural abnormalities
- X-linked inheritance patterns characteristic of this condition
Who Should Consider This Genetic Test
This comprehensive genetic screening is recommended for individuals presenting with:
- Unexplained developmental delays in childhood
- Intellectual disability of unknown origin
- Characteristic facial features associated with Wilson-Turner syndrome
- Family history suggestive of X-linked inheritance patterns
- Neurological symptoms without clear diagnosis
- Suspected genetic syndromes with overlapping features
Key Benefits of LAS1L Genetic Testing
Undergoing this advanced genetic analysis provides numerous advantages for patients and families:
- Accurate Diagnosis: Provides definitive genetic confirmation of Wilson-Turner syndrome
- Family Planning Guidance: Enables informed reproductive decisions through genetic counseling
- Personalized Treatment: Facilitates targeted interventions and management strategies
- Early Intervention: Allows for timely implementation of developmental support services
- Genetic Risk Assessment: Identifies carrier status in family members
Understanding Your Test Results
Our comprehensive genetic report provides clear interpretation of your results with guidance from our expert genetic counselors:
- Positive Result: Indicates the presence of a pathogenic LAS1L gene mutation, confirming Wilson-Turner syndrome diagnosis
- Negative Result: Suggests absence of detectable mutations in the LAS1L gene, though other genetic causes may need consideration
- Variant of Uncertain Significance: Identifies genetic changes requiring further clinical correlation and family studies
- Carrier Status: Determines if individuals carry the mutation without showing symptoms
Test Pricing Information
| Price Type | Amount (USD) |
|---|---|
| Discount Price | $500 |
| Regular Price | $700 |
Nationwide Testing Availability
GGC DNA maintains comprehensive testing facilities across the United States, with branches conveniently located in major metropolitan areas including New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, and San Jose. Our nationwide network ensures accessible genetic testing services for patients throughout the country.
Take Control of Your Genetic Health Today
Don’t let uncertainty about genetic conditions impact your family’s future. Our LAS1L Gene Wilson-Turner Syndrome NGS Genetic DNA Test provides the clarity and confidence you need for informed healthcare decisions. With results available in 3-4 weeks and multiple sample collection options including blood, extracted DNA, or blood spots on FTA cards, getting tested has never been more convenient.
Call or WhatsApp us today at +1(267) 388-9828 to schedule your genetic counseling session and book this essential diagnostic test. Our expert genetic counselors are available to answer your questions and guide you through the testing process.
