SLC2A5 Gene Fructose Uptake Deficiency NGS Genetic DNA Test
Comprehensive Genetic Analysis for Fructose Metabolism Disorders
The SLC2A5 Gene Fructose Uptake Deficiency NGS Genetic DNA Test represents a breakthrough in metabolic disorder diagnostics, specifically targeting the GLUT5 transporter encoded by the SLC2A5 gene. This specialized genetic test provides critical insights into fructose absorption mechanisms and identifies potential deficiencies that can significantly impact digestive health and overall metabolic function.
What Does This Test Measure and Detect?
This advanced genetic analysis utilizes Next-Generation Sequencing (NGS) technology to comprehensively examine the SLC2A5 gene for mutations and variations that affect fructose transport capabilities. The test specifically detects:
- Pathogenic variants in the SLC2A5 gene affecting GLUT5 transporter function
- Genetic mutations that impair intestinal fructose absorption
- Variations associated with primary fructose malabsorption
- Genetic markers for fructose transport deficiency disorders
- Inherited patterns of fructose metabolism abnormalities
Who Should Consider This Genetic Test?
This specialized genetic analysis is recommended for individuals experiencing:
- Unexplained gastrointestinal symptoms after consuming fruits or high-fructose foods
- Chronic bloating, abdominal pain, or diarrhea following fructose intake
- Family history of fructose intolerance or metabolic disorders
- Unexplained hypoglycemia episodes after fructose consumption
- Children with failure to thrive and digestive issues
- Individuals with suspected hereditary fructose metabolism disorders
- Patients with unexplained metabolic symptoms despite normal routine testing
Key Benefits of SLC2A5 Genetic Testing
Undergoing this comprehensive genetic analysis provides numerous advantages for patients and healthcare providers:
- Accurate Diagnosis: Provides definitive genetic confirmation of fructose uptake deficiency
- Personalized Treatment: Enables targeted dietary modifications and treatment strategies
- Family Planning: Identifies inheritance patterns for genetic counseling
- Symptom Management: Helps develop effective symptom management protocols
- Early Intervention: Allows for proactive management in at-risk family members
- Comprehensive Analysis: Utilizes advanced NGS technology for thorough genetic assessment
Understanding Your Test Results
Your genetic test results will provide clear, actionable information about your SLC2A5 gene status:
- Normal Result: No pathogenic variants detected in the SLC2A5 gene
- Pathogenic Variants: Identified mutations associated with fructose transport deficiency
- Variant of Uncertain Significance: Genetic changes requiring further clinical correlation
- Carrier Status: Identification of recessive inheritance patterns
All results include comprehensive interpretation by our genetic specialists and recommendations for next steps, including dietary modifications, follow-up testing, and specialist consultations when necessary.
Test Pricing and Availability
| Test Component | Price (USD) |
|---|---|
| Discount Price | $500 |
| Regular Price | $700 |
Nationwide Testing Availability
We have convenient testing locations across the United States, including major metropolitan areas such as New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, San Jose, and many other cities. Our network of certified collection centers ensures accessible testing for patients nationwide.
Take Control of Your Metabolic Health Today
Don’t let unexplained digestive symptoms or metabolic concerns go undiagnosed. Our SLC2A5 Gene Fructose Uptake Deficiency NGS Genetic DNA Test provides the answers you need for effective management of fructose-related metabolic disorders. With advanced NGS technology and expert genetic analysis, you can gain valuable insights into your metabolic health and develop targeted treatment strategies.
Ready to schedule your genetic test? Contact our genetic counseling team today at +1(267) 388-9828 or book your appointment online. Our specialists are available to answer your questions and guide you through the testing process.
Note: This test requires pre-test genetic counseling and clinical history assessment. Turnaround time is 3-4 weeks from sample receipt. Acceptable samples include blood, extracted DNA, or one drop of blood on FTA card.
