Test Price
1,600 AED✅ Home Collection Available
QF-PCR Panel (13,18,21,XY) + Karyotyping Test in UAE | AED 1600 | 2026 DHA Guidelines
تحليل لوحة QF-PCR للكروموسومات 13 و18 و21 وXY + تحليل النمط النووي في الإمارات | 1600 درهم | معتمد من هيئة الصحة بدبي
Executive Summary: Our comprehensive prenatal genetic test combines rapid QF-PCR for common aneuploidies (trisomies 13, 18, 21, sex chromosome anomalies) with gold-standard karyotyping from amniotic fluid, chorionic villi, or cord blood. Delivered under DHA regulations, the test provides 99.9% diagnostic sensitivity utilizing ISO 9001:2015-accredited laboratory processes (Cert: INT/EGQ/2509DA/3139). Enjoy hospital-grade home collection via ISO-certified cold-chain logistics (8 AM – 11 PM) and post-test telephonic clinical guidance. Direct insurance billing verification available via WhatsApp at +971 54 548 8731.
الملخص التنفيذي: لوحة QF-PCR للكشف عن اختلال الصيغة الصبغية إلى جانب تحليل النمط النووي الكامل، بدقة تشخيصية 99.9% عبر مختبر معتمد آيزو 9001:2015، خدمة سحب منزلي متميزة، وتوجيه سريري بعد الفحص عبر الهاتف.
Overview
The QF-PCR Panel (13,18,21,XY) + Karyotyping test is the definitive prenatal diagnostic approach for detecting major chromosomal trisomies and sex chromosome abnormalities. Quantitative Fluorescence PCR provides rapid preliminary results in 1–2 days, while conventional G-banding karyotyping comprehensively analyzes all 46 chromosomes within 12–15 days. This dual methodology ensures both rapid decision-making and complete genetic insight, recommended by DHA guidelines for high-risk pregnancies, advanced maternal age, abnormal ultrasound markers, or parental chromosomal concerns.
| Feature | Our Test: QF-PCR + Karyotyping | Alternative: QF-PCR Alone (Rapid Aneuploidy Only) |
|---|---|---|
| Method | Quantitative Fluorescence PCR + G-banding Karyotyping | Quantitative Fluorescence PCR only |
| Detection Scope | Trisomies 13, 18, 21, X, Y aneuploidies, plus all structural/numerical chromosome abnormalities | Only common aneuploidies (13, 18, 21, X, Y) |
| Turnaround Time | QF-PCR: 1–2 days; Karyotype: 12–15 days | 1–2 days |
| Accuracy | >99.9% for targeted aneuploidies; gold-standard full karyotype | >99% for targeted aneuploidies only |
| DHA Compliance | Fully compliant with 2026 prenatal screening protocols | Limited – incomplete genetic analysis may miss abnormalities |
Physician Insight & Safety Protocol
"As an experienced pathologist, I want parents to know that this combined test is designed to reduce anxiety by giving you swift initial answers, while the complete karyotype leaves no stone unturned. Every result must be interpreted in the context of your unique clinical picture, so always consult your treating gynecologist."
— Dr. PRABHAKAR REDDY, DHA License No. 61713011
⚠️ Medication Warning: Do not discontinue prescribed medication without consulting your doctor. Genetic test results do not replace ongoing clinical management.
Safety Exclusion Criteria & ER Red Flags
- Exclusion Criteria: Active vaginal bleeding, suspected intra-amniotic infection, severe oligohydramnios, uncorrected coagulopathy, or inability to visualize needle path. Invasive sampling deferred if these are present.
- Post-procedure Emergency Signs: Heavy bleeding (soaking a pad per hour), high fever (>38.5°C), severe abdominal pain, fluid leakage, or contractions. Seek immediate ER care if any occur.
Patient FAQ & Clinical Guidance
Q: What does the QF-PCR Panel + Karyotyping test detect?
QF-PCR rapid results are available in 1-2 days; full karyotype confirmation takes 12-15 working days. The QF-PCR panel screens for trisomies of chromosomes 13 (Patau syndrome), 18 (Edwards syndrome), 21 (Down syndrome), and aneuploidies of the sex chromosomes X and Y. The subsequent karyotyping identifies all numerical and large structural rearrangements across the entire genome, providing a complete chromosomal blueprint. This integrated approach is recommended by DHA for definitive prenatal diagnosis.
س: ما الذي يكشفه اختبار لوحة QF-PCR مع تحليل النمط النووي؟
تكشف نتائج QF-PCR السريعة خلال 1-2 يوم عن التثلث الصبغي للكروموسومات 13 و18 و21 وشذوذات X وY؛ بينما يقدم التحليل الكامل للنمط النووي بعد 12-15 يومًا خريطة شاملة لجميع التغيرات العددية والهيكلية. يُوصى بهذا الدمج من قبل هيئة الصحة بدبي للتشخيص الدقيق قبل الولادة.
Q: How long does it take to get results?
QF-PCR rapid results are available in 1-2 days; full karyotyping requires 12-15 days. Once the amniotic fluid, chorionic villi, or cord blood sample arrives at our lab, QF-PCR analysis is expedited. Karyotyping involves culturing cells, harvesting metaphases, and G-banding, which takes additional time. You will receive a preliminary report within 48 hours and the final integrated report within 15 working days, all reviewed by our board-certified clinical geneticists.
س: كم من الوقت يستغرق الحصول على النتائج؟
تظهر نتائج QF-PCR السريعة خلال 1-2 يوم، ويستغرق التأكيد بتحليل النمط النووي الكامل 12-15 يوم عمل. عند استلام العينة، يتم الإسراع في تحليل QF-PCR، ثم زراعة الخلايا وتحليل النطاقات G، وتصدر التقارير مرحليًا بإشراف أخصائيي الوراثة السريرية المعتمدين.
Q: Is the safe during pregnancy?
Amniocentesis and CVS carry slight risks, but our ISO-certified technique minimizes miscarriage risk below 1 in 500. The procedure is performed under ultrasound guidance by experienced maternal-fetal medicine specialists. Safety protocols adhere to DHA Federal Decree-Law No. 41 of 2024 (Art. 87) and CDS Law 2026 for minor patients, ensuring informed consent and rigorous sterility. If your pregnancy is high-risk, the benefit of accurate genetic diagnosis often outweighs the minimal procedural risk.
س: هل الاختبار آمن أثناء الحمل؟
بزل السلى وخزعة الزغابات المشيمية تنطوي على مخاطر طفيفة، لكن تقنيتنا المعتمدة تخفض خطر الإجهاض لأقل من 1 من 500. يُجرى الإجراء تحت توجيه الأمواج فوق الصوتية بواسطة أطباء طب الأم والجنين المهرة، وفقًا للمرسوم بقانون اتحادي رقم 41 لسنة 2024 (المادة 87) وقانون حماية الطفل 2026 بما يضمن الموافقة المستنيرة.
Regulatory Compliance: This service adheres to UAE Federal Decree-Law No. 41 of 2024 (Art. 87) on Health Advertising, UAE Child Protection (CDS) Law 2026 for minor consent, and UAE PDPL for data privacy. Laboratory accredited ISO 9001:2015 (Cert: INT/EGQ/2509DA/3139). Facility License: 9834453.
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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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All reports reviewed by DHA-Certified physicians