SLC4A1 Gene Ovalocytosis NGS Genetic DNA Test
Comprehensive Genetic Analysis for Hereditary Ovalocytosis
The SLC4A1 Gene Ovalocytosis NGS Genetic DNA Test represents a breakthrough in molecular diagnostics for inherited blood disorders. This advanced genetic test specifically targets the SLC4A1 gene, which encodes the band 3 protein essential for red blood cell membrane stability and function. Hereditary ovalocytosis is an autosomal dominant condition characterized by elliptical or oval-shaped red blood cells, leading to various clinical manifestations ranging from asymptomatic carriers to significant hemolytic anemia.
What This Test Measures and Detects
Our sophisticated NGS technology provides comprehensive analysis of the SLC4A1 gene to identify:
- Point mutations affecting band 3 protein structure
- Deletion and insertion variants in the SLC4A1 gene
- Genetic polymorphisms associated with ovalocytosis
- Specific mutations causing Southeast Asian ovalocytosis
- Variants affecting anion exchange function in erythrocytes
Who Should Consider This Test
This genetic test is recommended for individuals experiencing:
- Unexplained hemolytic anemia symptoms
- Family history of hereditary ovalocytosis
- Abnormal peripheral blood smear showing ovalocytes
- Recurrent anemia without clear etiology
- Symptoms affecting multiple organ systems including liver, kidney, and endocrine function
- Ethnic background with higher prevalence (Southeast Asian, Melanesian populations)
Clinical Benefits of Genetic Testing
Undergoing the SLC4A1 Gene Ovalocytosis test provides numerous advantages:
- Accurate Diagnosis: Confirm hereditary ovalocytosis with molecular precision
- Personalized Treatment: Guide therapeutic decisions based on genetic findings
- Family Planning: Understand inheritance patterns for future generations
- Risk Assessment: Identify asymptomatic carriers within families
- Comprehensive Care: Coordinate management across hepatology, nephrology, and endocrinology specialties
Understanding Your Test Results
Our genetic counseling team provides detailed interpretation of your results:
- Positive Result: Identifies specific SLC4A1 mutation confirming hereditary ovalocytosis diagnosis
- Negative Result: Rules out common SLC4A1 mutations associated with ovalocytosis
- Variant of Uncertain Significance: Requires additional family studies and clinical correlation
- Carrier Status: Identifies individuals with single mutation copy who may pass condition to offspring
Test Pricing Information
| Test Description | Price (USD) |
|---|---|
| SLC4A1 Gene Ovalocytosis NGS Genetic DNA Test – Discount Price | $500 |
| SLC4A1 Gene Ovalocytosis NGS Genetic DNA Test – Regular Price | $700 |
Nationwide Testing Availability
General Genetics Corporation provides comprehensive genetic testing services across the United States. We have established branches in all major metropolitan areas including New York City, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, San Jose, and many other locations. Our network ensures accessible genetic testing with consistent quality standards nationwide.
Take Control of Your Genetic Health
Don’t let uncertainty about hereditary conditions affect your health decisions. Our SLC4A1 Gene Ovalocytosis NGS Genetic DNA Test provides the clarity you need for informed medical management. 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 us today at +1(267) 388-9828 to schedule your genetic counseling session and book your test. Our genetic specialists are ready to guide you through the testing process and help you understand your results for better health outcomes.
Remember to bring your clinical history and be prepared for a genetic counseling session to create a detailed family pedigree chart. This comprehensive approach ensures the most accurate interpretation of your genetic results and personalized recommendations for your specific situation.
