Test Price
2,400 AED✅ Home Collection Available
NIPT Microdeletion Screening – Advanced Fetal Genetic Analysis in Dubai
Executive Summary & Core Metrics
- Diagnostic Accuracy >99% – Next-generation sequencing (NGS) detects clinically significant microdeletions with high sensitivity.
- VIP Mobile Phlebotomy – Temperature-controlled cold-chain home collection available daily 8 AM–11 PM.
- Post-Result Genetic Counselling – Personalised telephonic guidance from our Consultant Medical Genetics.
- Direct Insurance Billing – Verify coverage via WhatsApp +971 54 548 8731.
Test Overview & Methodology
This non-invasive prenatal screening extends beyond common trisomies to detect microdeletion syndromes such as 22q11.2 deletion (DiGeorge), 1p36 deletion, Cri-du-Chat, Prader-Willi/Angelman, and Wolf-Hirschhorn. Using next-generation sequencing of cell-free fetal DNA from maternal blood, results are available in 8–10 working days. The test is suitable for singleton pregnancies ≥10 weeks gestation.
| Feature | Our NIPT Microdeletion Panel | Standard NIPT (Trisomies Only) |
|---|---|---|
| Technology | Next-Generation Sequencing with full microdeletion analysis | NGS limited to aneuploidy (21, 18, 13) |
| Detection Scope | 22q11.2, 1p36, Cri-du-Chat, Prader-Willi/Angelman, Wolf-Hirschhorn, and additional microdeletions | Trisomies 21, 18, 13 (sex chromosome optional) |
| Turnaround Time | 8–10 working days | 5–7 working days |
| Clinical Utility | Early detection of severe neurodevelopmental disorders | Common aneuploidy screening only |
Physician Insight & Safety Protocols
“NIPT microdeletion screening provides valuable insight into fetal chromosomal architecture, but it remains a screening test. A positive result requires confirmatory invasive testing such as amniocentesis or chorionic villus sampling. Always interpret results in the context of maternal age, ultrasound findings, and family history.”
— Lina Osama Zaki Quteineh, Consultant Medical Genetics (DHA 9294403)
⚠️ Important Advisory
Do not discontinue any prescribed medication without consulting your physician. This blood test does not require any medication changes. Any alteration to your treatment regimen may affect maternal or fetal health.
Exclusion Criteria & Urgent Red Flags
- Multiple gestation beyond twins (requires specialist counselling)
- Gestational age less than 10 weeks at blood draw
- Maternal history of malignancy or active neoplasia
- History of recent blood transfusion or immunotherapy
ER Red Flags – Seek immediate care if you experience:
- Heavy vaginal bleeding (soaking a pad per hour)
- Severe abdominal pain or cramping
- Sudden gush of fluid or loss of pregnancy symptoms
Patient FAQ & Clinical Guidance
1. What exactly does the NIPT Microdeletion screen look for?
This non-invasive screening analyzes fetal cell-free DNA in maternal blood to detect the most clinically significant microdeletion syndromes—such as 22q11.2 deletion (DiGeorge) and 1p36 deletion—with high specificity. It is designed to complement standard trisomy screening.
2. How reliable is a “high-risk” result, and what happens next?
A high-risk result indicates increased probability but is not diagnostic; confirmatory invasive testing (amniocentesis or CVS) is mandatory before any clinical decision. Our genetics team will guide you through the next steps.
3. Can I use insurance to cover the 3000 AED cost?
Coverage varies by policy; our team verifies eligibility via WhatsApp (+971 54 548 8731) and supports direct billing with major UAE insurers. Please contact us before booking.
4. Is home blood collection available for this test?
Yes, our VIP Mobile Phlebotomy service is available daily from 8 AM to 11 PM. Samples are collected under strict temperature-controlled cold-chain conditions for optimal DNA preservation.
UAE Regulatory & Data Privacy Adherence
DNA Labs UAE complies 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 testing safety and patient consent adhere to Federal Decree-Law No. 4 of 2016 on Medical Liability. Your genetic data is encrypted, access-controlled, and never shared without explicit consent.
Clinical & Logistical Metadata
| Test Name | NIPT Microdeletion Screening (22q11.2, 1p36, Cri-du-Chat, Prader-Willi/Angelman, Wolf-Hirschhorn & more) |
| Price (AED) | 3,000 AED |
| Turnaround Time | 8–10 working days |
| Sample Type / Matrix | Peripheral whole blood (maternal venous blood) |
| Methodology Used | Next-Generation Sequencing (NGS) – cell-free fetal DNA analysis |
| ICD-10-CM Code | Z36.2 (Encounter for antenatal screening for chromosomal anomalies) |
| LOINC Code | 82659-0 (Noninvasive prenatal genomic analysis by NGS) |
| DHA Facility License & Address | DHA License #1143 | Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE |
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