SLC2A5 Gene Fructose Uptake Deficiency SLC2A5 Related NGS Genetic DNA Test
Introduction to the Test
The SLC2A5 Gene Fructose Uptake Deficiency SLC2A5 Related NGS Genetic DNA Test is a specialized diagnostic tool that employs Next Generation Sequencing (NGS) technology to identify mutations in the SLC2A5 gene, which plays a critical role in fructose metabolism. This test is essential for diagnosing fructose uptake deficiency, a metabolic disorder that can lead to severe health complications if left unmanaged.
What the Test Measures
This genetic test measures the presence of specific mutations in the SLC2A5 gene, which is responsible for encoding the transporter protein that facilitates fructose uptake in the intestines. By identifying these mutations, healthcare providers can better understand a patient’s metabolic capabilities and tailor treatment plans accordingly.
Who Should Consider This Test?
Individuals who experience symptoms such as:
- Abdominal pain after consuming fructose
- Nausea and vomiting
- Diarrhea
- Failure to thrive in infants
- Symptoms of metabolic disorders
Additionally, those with a family history of fructose intolerance or metabolic disorders may benefit from this test.
Benefits of Taking the Test
- Early diagnosis of fructose uptake deficiency can prevent serious health issues.
- Informs dietary and lifestyle changes to avoid fructose-related complications.
- Provides valuable information for family planning and genetic counseling.
- Helps healthcare providers create personalized treatment plans.
Understanding Your Results
Results from the SLC2A5 Gene Fructose Uptake Deficiency test will indicate whether any mutations were detected. A positive result suggests a genetic predisposition to fructose intolerance, while a negative result may rule out the condition. It is crucial to discuss results with a healthcare professional for appropriate interpretation and guidance.
Test Pricing
| Test Name | Price (KSh) |
|---|---|
| Discount Price | 40,000 |
| Regular Price | 56,000 |
Additional Information
The turnaround time for results is approximately 3 to 4 weeks. Samples can be collected through blood, extracted DNA, or a single drop of blood on an FTA card. Prior to testing, a genetic counseling session is recommended to create a pedigree chart of family members affected by fructose uptake deficiency.
We have branches across major cities in Kenya, making it convenient for you to access our services. For more information or to book your test, please call or WhatsApp us at +254711564616.
