FOXN1 Gene T-Cell Immunodeficiency, Congenital Alopecia and Nail Dystrophy NGS Genetic DNA Test
Understanding FOXN1 Gene Disorders
The FOXN1 gene plays a critical role in the development and function of the immune system, particularly in the formation of T-cells, which are essential for fighting infections and maintaining immune health. Mutations in this gene can lead to a rare genetic condition characterized by three primary features: severe T-cell immunodeficiency, congenital alopecia (complete absence of hair from birth), and nail dystrophy (abnormal nail development). This comprehensive NGS genetic DNA test provides definitive diagnosis and crucial information for managing this complex disorder.
What This Test Detects
Our advanced Next-Generation Sequencing (NGS) technology specifically targets and analyzes the FOXN1 gene to identify pathogenic variants that cause:
- Mutations affecting thymic epithelial cell development
- Genetic alterations disrupting T-cell maturation
- Variants responsible for congenital hair follicle abnormalities
- Genetic changes causing nail matrix development issues
- Inherited patterns of immune system dysfunction
Who Should Consider This Test
Clinical Indications and Symptoms
This genetic test is recommended for individuals presenting with:
- Complete absence of hair (alopecia) present from birth
- Recurrent, severe infections starting in infancy
- Abnormal nail development and growth patterns
- Family history of immune deficiency disorders
- Unexplained failure to thrive in infancy
- Multiple hospitalizations for infections
- Developmental delays associated with immune dysfunction
Benefits of FOXN1 Genetic Testing
Undergoing this comprehensive genetic analysis provides numerous advantages:
- Accurate Diagnosis: Confirms or rules out FOXN1-related disorders with high precision
- Personalized Treatment: Enables targeted immune therapy and management strategies
- Family Planning: Provides crucial information for genetic counseling and reproductive decisions
- Early Intervention: Facilitates prompt treatment to prevent serious complications
- Comprehensive Care: Guides multidisciplinary approach involving dermatology, immunology, and genetics specialists
Understanding Your Test Results
Our genetic specialists provide detailed interpretation of your FOXN1 gene analysis:
- Positive Result: Indicates the presence of pathogenic FOXN1 mutations, confirming diagnosis and guiding treatment
- Negative Result: Suggests FOXN1 mutations are not the cause of symptoms, directing further diagnostic evaluation
- Variant of Uncertain Significance: Identifies genetic changes requiring additional family studies for clarification
- Carrier Status: Determines if individuals carry one copy of mutated gene without showing symptoms
Test Pricing and Details
| Test Feature | Details |
|---|---|
| Test Name | FOXN1 Gene T-Cell Immunodeficiency, Congenital Alopecia and Nail Dystrophy NGS Genetic DNA Test |
| Discount Price | $500 USD |
| Regular Price | $700 USD |
| Turnaround Time | 3 to 4 Weeks |
| Sample Type | Blood, Extracted DNA, or One Drop Blood on FTA Card |
Nationwide Testing Availability
We have diagnostic centers conveniently located across the United States, serving major metropolitan areas including New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, and San Jose. Our network ensures accessible genetic testing services for patients nationwide.
Take Control of Your Genetic Health
Don’t let uncertainty about immune disorders and genetic conditions affect your quality of life. Our FOXN1 genetic test provides the clarity needed for proper diagnosis and effective treatment planning. With our discounted price of $500 USD and comprehensive genetic counseling support, you can make informed decisions about your health and future.
Ready to schedule your genetic test? Call or WhatsApp us today at +1(267) 388-9828 to book your appointment and take the first step toward understanding your genetic health.
