Test Price
2,800 AED✅ Home Collection Available
SLC5A2 Gene Renal Glucosuria Genetic Test in UAE | 2,800 AED | 2026 DHA Guidelines
تحليل جين SLC5A2 للبيلة السكرية الكلوية بتقنية التسلسل الجيني الشامل (NGS) في الإمارات | 2,800 درهم | معتمد من هيئة الصحة بدبي
Executive Summary
This NGS‑based SLC5A2 gene test provides definitive diagnosis of familial renal glucosuria with 99.9% analytical sensitivity. It is performed under ISO 9001:2015 certified protocols, includes home collection via cold‑chain VIP phlebotomy (8 AM‑11 PM), and comes with a mandatory genetic counselling session and a post‑result telehealth consultation. Direct insurance billing verification is available through WhatsApp at +971 54 548 8731.
ملخص تنفيذي: يكشف هذا الاختبار بدقة تبلغ 99.9% عن الطفرات المسببة للبيلة السكرية الكلوية العائلية في جين SLC5A2، ويتم وفق معايير ISO 9001:2015 مع خدمة سحب منزلي متطورة (سلسلة تبريد معتمدة) واستشارة وراثية قبل وبعد النتيجة.
🔬 Clinical & Technical Overview
The SLC5A2 gene test uses next‑generation sequencing (NGS) to identify pathogenic variants in the renal sodium‑glucose cotransporter gene, confirming autosomal recessive familial renal glucosuria. It differentiates this benign condition from diabetes mellitus and other tubulopathies, providing clarity for patient management and family planning.
| Feature | Our NGS Panel (UAE) | Closest Alternative (Conventional) |
|---|---|---|
| Precision | Full gene sequencing + CNV analysis | Limited Sanger sequencing of hot‑spot exons |
| Method | Illumina NGS (verified by LC‑MS/MS validation) | Single‑gene Sanger |
| Turnaround | 3–4 Weeks | 6–8 Weeks |
🩺 Physician Insight & Safety Protocol
“As a clinician, I see the SLC5A2 test as a powerful tool to rule out a benign cause of persistent glucosuria, but it must never replace a thorough metabolic evaluation. A positive result confirms renal glucose wasting without hyperglycemia; however, always cross‑reference with fasting blood glucose, HbA1c, and renal function tests. Genetic data alone cannot capture all aspects of your health.”
— Dr. PRABHAKAR REDDY, DHA License: 61713011
⚕️ Do not discontinue prescribed medication without consulting your doctor.
🚨 Critical Safety Alerts
- Exclusion Criteria: Patients with acute febrile illness, active haemodynamic instability, or inability to provide informed consent (guardian required for minors under UAE CDS Law 2026).
- ER Red Flags: Massive polyuria leading to dehydration, profound electrolyte imbalances (hypokalemia, hyponatremia), or sudden altered mental status require immediate hospital evaluation — do not rely solely on this genetic report.
- All genetic counselling sessions are mandatory per DHA/MOHAP regulations; results will be released only after post‑test counselling.
❓ Patient FAQ & Clinical Guidance
1. What exactly does the SLC5A2 gene renal glucosuria test detect?
Snippet: The SLC5A2 gene renal glucosuria is a comprehensive NGS assay that identifies pathogenic mutations in the SLC5A2 gene responsible for familial renal glucosuria, a hereditary condition causing glucose in urine despite normal blood sugar levels.
(يكشف فحص جين SLC5A2 عن الطفرات المسببة للبيلة السكرية الكلوية الوراثية).
2. How is the sample collected and is home service available?
Snippet: A trained DHA‑licensed phlebotomist draws a standard blood sample or a finger‑prick dried blood spot on an FTA card in your home, transported under ISO‑certified cold‑chain conditions between 8 AM and 11 PM daily.
(يتم سحب العينة منزلياً بواسطة ممرض معتمد ونقلها بسلسلة تبريد).
3. When will I receive my results and what support is provided?
Snippet: Your personalised genetic report, reviewed by our clinical geneticist, is delivered within 3 to 4 weeks along with a complimentary telehealth session to interpret the findings and guide next steps.
(تصلك النتيجة خلال 3-4 أسابيع مع جلسة استشارية عن بعد).
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ISMS 27001:2022
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All reports reviewed by DHA-Certified physicians