Test Price
100 AED✅ Home Collection Available
Alpha Fetoprotein (AFP) Amniotic Fluid Test in UAE | 100 AED
Executive Summary & Core Metrics
This test offers 99.9% diagnostic sensitivity with DHA-compliant hospital extraction, post-test clinical guidance, and direct insurance verification.
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 Accredited Processing (Cert: INT/EGQ/2509DA/3139).
- Premium Logistics: Hospital Extraction Only – Sample collection is conducted strictly within an accredited hospital facility; mobile home phlebotomy is disabled for safety. Cold-chain transport to ISO-certified lab.
- Clinical Guidance: Telephonic post-test clinical guidance in result interpretation by DHA-licensed clinicians.
- Insurance: Direct billing verification via WhatsApp +971 54 548 8731.
Test Overview & Methodology
The Alpha Fetoprotein (AFP) Amniotic Fluid Test quantitatively measures alpha-fetoprotein levels in amniotic fluid to screen for open neural tube defects (spina bifida, anencephaly) and chromosomal anomalies during pregnancy. Paired with high-resolution ultrasound, it delivers essential prenatal diagnostic insights compliant with DHA/MOHAP screening protocols.
| Feature | Our UAE Test (CLIA, ISO) | Closest Alternative (ELISA/RIA) |
|---|---|---|
| Methodology | Ultra-Sensitive Chemiluminescent Immunoassay (CLIA) – high specificity, low cross-reactivity | Legacy ELISA or RIA; higher interference risk |
| Precision / LoD | 99.9% diagnostic sensitivity; ISO 9001:2015 validated | Typically 85-94% sensitivity; method-dependent |
| Turnaround Time | Same-day (daily batch runs) | 2-3 days |
| Sample Handling | ISO 15189 cold-chain, sterile container; maternal blood avoidance protocol | Often room temperature; no dedicated contamination checks |
| Regulatory Compliance | Full DHA/MOHAP, Federal Decree-Law No. 45 of 2021 (PDPL), Federal Law No. 2 of 2019 (Health ICT) | May not meet post-2021 UAE data protection laws |
Physician Insight & Safety Protocols
“Elevated amniotic fluid AFP must be correlated with targeted fetal ultrasound and genetic counselling. This assay provides outstanding screening accuracy, but definitive diagnosis requires a complete clinical picture. Always interpret results together with your obstetrician-geneticist team.”
— Lina Osama Zaki Quteineh, Consultant Medical Genetics, DHA Registration ID: 9294403
⚠️ Medication & Discontinuation Warning
Do not discontinue any prescribed medication without consulting your treating physician. This test is part of a prenatal screening program and not a standalone decision tool.
Safety Protocol & Exclusion Criteria
- Maternal blood contamination invalidates sample; ensure strictly amniotic fluid collection under ultrasound guidance.
- If amniocentesis performed, monitor for signs of infection, fluid leakage, severe abdominal pain, or vaginal bleeding – seek immediate emergency care.
- Not for use as a sole diagnostic tool; confirmatory procedures (amniocentesis karyotyping, high-resolution ultrasound) are mandatory.
- Do not perform in pregnancies with known placenta previa or bleeding disorders without specialist clearance.
- Results interpretation must follow Federal Decree-Law No. 4 of 2016 on Medical Liability; parental consent and counselling are required.
Patient FAQ & Clinical Guidance
1. What is the cost and turnaround time for the AFP Amniotic Fluid Test in UAE?
The test costs 100 AED with same-day daily results, ensuring rapid prenatal screening without delay. We process samples 7 days a week, enabling your obstetrician to make timely clinical decisions. The price includes sterile container, cold-chain transport, and ISO-accredited laboratory analysis. For exact timing on the day of amniocentesis, coordinate with our hospital extraction team via WhatsApp.
2. How accurate is the AFP Amniotic Fluid test compared to other methods?
Our UAE-based ISO-certified chemiluminescent assay achieves 99.9% diagnostic sensitivity for neural tube defect screening, surpassing older ELISA methods. The ultra-sensitive CLIA platform minimizes false positives from maternal blood proteins and provides reproducible results. Paired with ultrasound, detection rates for open spina bifida exceed 96%, aligning with DHA prenatal screening benchmarks.
3. Is the AFP Amniotic Fluid test safe during pregnancy?
Yes, when performed by a qualified specialist via ultrasound-guided amniocentesis, the procedure carries low risk. Our medical team in the UAE adheres to DHA licensing and safety standards. The sample collection and handling follow rigorous protocols to ensure maternal and fetal safety.
For any clinical queries or to schedule a hospital extraction, Contact us on WhatsApp at +971 54 548 8731.
UAE Regulatory & Data Privacy Adherence
This laboratory test is fully compliant with Federal Decree-Law No. 45 of 2021 on Personal Data Protection (PDPL) and Federal Law No. 2 of 2019 Concerning the Use of Information and Communication Technology in Health Fields. All clinical procedures adhere to Federal Decree-Law No. 4 of 2016 on Medical Liability, ensuring patient safety, informed consent, and medico-legal accountability. DNA Labs UAE operates under DHA License No. 1143 and ISO 9001:2015 certification.
Clinical & Logistical Metadata
| Metadata Field | Value |
|---|---|
| Test Name | Alpha Fetoprotein (AFP) Amniotic Fluid Test |
| Price (AED) | 100 AED |
| Turnaround Time | Same-day (daily batch runs) |
| Sample Type / Matrix | Amniotic Fluid (3 mL) – Hospital Extraction Only |
| Methodology Used | Ultra-Sensitive Chemiluminescent Immunoassay (CLIA) |
| ICD-10-CM Code | O35.8 (Maternal care for other fetal abnormality) |
| LOINC Code | 1834-1 (Alpha-1-fetoprotein [Mass/volume] in Amniotic fluid) |
| DHA Facility License & Laboratory Address | DNA Labs UAE, DHA License No. 1143, Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE |
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