Test Price
5,000 AED✅ Home Collection Available
Glucose-6-Phosphate Dehydrogenase (G6PD) Full Length Gene Sequence Analysis in UAE | 5000 AED | 2026 DHA Guidelines
تحليل تسلسل جين G6PD الكامل في الإمارات | 5000 درهم | معتمد من هيئة الصحة بدبي 2026
تحليل جيني دقيق بمعايير عالمية للكشف عن طفرات G6PD، مُعتمد من هيئة الصحة بدبي مع خدمة سحب منزلية واستشارة طبية هاتفية.
Overview
The G6PD full-length gene sequence analysis is the most comprehensive genetic test for detecting mutations causing Glucose-6-Phosphate Dehydrogenase deficiency. It sequences every exon of the G6PD gene using Sanger sequencing, providing a definitive molecular diagnosis for lifelong hemolytic anemia risk, often recommended by gynecologists, diabetologists, and general physicians for at-risk individuals and families.
| Feature | Our Test (G6PD Full Gene Sequence) | Closest Alternative (Enzyme Activity Assay) |
|---|---|---|
| Precision | Single‑nucleotide resolution – identifies exact mutation | Quantitative enzyme level; may miss heterozygous females |
| Method | Sanger Sequencing (gold standard) | Spectrophotometric enzyme assay |
| Turnaround | 2–3 weeks | 1–2 days |
| Clinical Impact | Lifetime diagnosis and genetic counseling | Acute episode assessment only; false‑normal in reticulocytosis |
Physician Insight & Safety Protocol
“The G6PD full gene sequence test offers a definitive molecular blueprint, essential for accurate diagnosis and family screening. While the test detects known pathogenic variants with high precision, clinical correlation with hemolytic episodes and enzyme activity remains vital. Always discuss the results with your DHA‑licensed physician before altering any treatment plan.”
– Dr. PRABHAKAR REDDY, DHA License: 61713011
Important Medication Warning
Do not discontinue prescribed medication without consulting your doctor. G6PD deficiency may require avoidance of certain drugs (e.g., sulfonamides, dapsone, primaquine), but only a licensed clinician can safely adjust your regimen after reviewing genetic results.
Safety Exclusion Criteria & ER Red Flags
- Exclusion: Test not recommended within 3 months of a blood transfusion, as donor DNA may confound results.
- ER Red Flags: If you experience sudden dark urine, jaundice, extreme fatigue, or back pain after exposure to triggers (fava beans, certain medications), seek emergency care immediately.
Patient FAQ & Clinical Guidance
1. What is the G6PD full gene test and why is it necessary?
The test sequences the entire G6PD gene to identify inherited mutations that cause enzyme deficiency, thereby confirming susceptibility to hemolytic anemia, guiding medication and dietary precautions.
يقوم التحليل بتسلسل كامل جين G6PD لاكتشاف الطفرات الوراثية المسببة لنقص الإنزيم، مما يؤكد القابلية للإصابة بفقر الدم الانحلالي ويوجه تجنب الأدوية والأطعمة المؤثرة.
2. How is the sample collected, and is home collection available?
A small blood, amniotic fluid, or cord blood sample is collected painlessly; VIP home collection by certified phlebotomists is available from 8 AM to 11 PM with guaranteed cold‑chain transport.
يتم سحب عينة صغيرة من الدم أو السائل الأمنيوسي أو دم الحبل السري بطريقة غير مؤلمة؛ وتتوفر خدمة السحب المنزلي المميزة من الساعة 8 صباحاً حتى 11 مساءً مع نقل مبرد مضمون.
3. What do the results mean and how long do they take?
Results in 2–3 weeks will indicate whether you carry a pathogenic variant; a negative result does not completely rule out G6PD deficiency if enzyme activity remains low for other reasons.
تظهر النتائج خلال 2-3 أسابيع ما إذا كنت تحمل طفرة مرضية؛ والنتيجة السلبية لا تستبعد بالكامل نقص الإنزيم إذا ظل النشاط الأنزيمي منخفضاً لأسباب أخرى.
Legal Compliance: This service adheres to Federal Decree-Law No. 41 of 2024 on Medical Liability (Art. 87), UAE PDPL (Data Privacy), and CDS Law 2026 for minors’ consent. methodology is validated under ISO 9001:2015 certification. Contact WhatsApp +971 54 548 8731 for insurance direct billing.
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توقف عن التخمين. أرسل صورة من بطاقة التأمين ووصفة الطبيب إلى فريق التحقق المعتمد من هيئة الصحة بدبي عبر الواتساب. احصل على تحديث الحالة في دقائق.
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