Test Price
480 AED✅ Home Collection Available
High‑Resolution Neonatal Chromosome Analysis (Karyotyping) in UAE | 480 AED | 2026 DHA Guidelines
تحليل الكروموسومات عالي الدقة لحديثي الولادة في الإمارات | 480 درهم | معتمد من هيئة الصحة بدبي
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015‑accredited cytogenomic processing (Cert: INT/EGQ/2509DA/3139).
- Premium Logistics: Paid Hospital‑Grade Home Collection with ISO‑certified cold‑chain transport (2‑8°C) and VIP Mobile Phlebotomy for your newborn.
- Clinical Guidance: Telephonic Post‑Test Clinical Interpretation by a DHA‑licensed specialist to explain karyotype results and next steps.
- Insurance: Direct Billing Verification via WhatsApp: +971 54 548 8731
Test Overview
High‑Resolution Neonatal Chromosome Analysis (Karyotyping) detects numerical and structural chromosome abnormalities in newborns with a banding resolution of ≥550 bands, enabling identification of subtle microdeletions or duplications. This test uses cultured peripheral blood lymphocytes and GTG‑banding to provide a definitive cytogenetic diagnosis for suspected congenital disorders.
يكشف تحليل الكروموسومات عالي الدقة لحديثي الولادة عن الاضطرابات العددية والتركيبية للكروموسومات بدقة تفوق 550 نطاقاً، مما يساعد في تشخيص المتلازمات الخلقية بدقة عالية.
| Feature | Our Test (High‑Resolution Karyotype) | Closest Alternative (Routine Karyotype) |
|---|---|---|
| Band Resolution | ≥550 bands (HRK) | 400–500 bands |
| Methodology | Culture + GTG‑banding + digital microscopy | Culture + basic Giemsa banding |
| Turnaround Time | 21 working days | 10–14 working days (lower resolution) |
| Clinical Application | Neonatal dysmorphism, multiple congenital anomalies, ambiguous genitalia | General pediatric screening, lower sensitivity |
Physician Insight & Safety Protocol
“A high‑resolution karyotype is a powerful tool when a newborn presents with physical or developmental findings that raise suspicion for a chromosomal syndrome. I always remind parents that an abnormal result requires careful clinical correlation, and a normal result does not exclude all genetic conditions – it simply tells us the chromosome structure looks intact at this level of detail. We use this result alongside clinical examination, newborn screening, and, if indicated, chromosomal microarray to give you the most complete picture.”
— Dr. PRABHAKAR REDDY, DHA License No. 61713011 (Consultant Pediatrician & Neonatologist)
⚠️ Medication Warning: Do not discontinue, modify, or withhold any prescribed medication for your newborn without direct consultation with the treating physician. This test does not replace urgent clinical management.
Exclusion Criteria & Emergency Red Flags
- Exclusion: Neonates with acute severe sepsis, hemodynamic instability, or severe coagulopathy where blood draw poses a risk.
- Exclusion: Inability to obtain the mandatory, fully completed Chromosome & FISH Analysis Requisition Form (Form 17).
- Emergency Red Flags: If your newborn has persistent cyanosis, seizures, severe hypotonia, or critical cardiac symptoms, proceed to the nearest emergency department – do not wait for test results.
Patient FAQ & Clinical Guidance
What does a high‑resolution neonatal karyotype detect, and how is it different from a standard chromosome test?
A high‑resolution neonatal karyotype detects chromosomal numerical and structural abnormalities – such as trisomies, translocations, deletions, and duplications – at a much finer level of detail than a standard test, using extended culture and high‑resolution banding to achieve ≥550 bands per haploid set.
يكشف النمط النووي عالي الدقة عن التثلث الصبغي والانتقالات والحذف والتضاعف بدقة تفوق 550 نطاقاً، مما يمكّن من رؤية تغييرات صغيرة لا تظهر في التحليل التقليدي.
How is the blood collection done for a newborn, and will it hurt my baby?
Our pediatric phlebotomists use ultra‑fine butterfly needles, topical numbing cream, and non‑invasive comforting techniques to collect the minimal 2 mL of blood in a sodium heparin tube, making the procedure swift and as gentle as possible for your newborn.
يستخدم خبراء سحب الدم للأطفال إبراً فائقة النعومة وكريم مخدر وتقنيات تهدئة مريحة لسحب 2 مل من الدم في أنبوب الهيبارين الصوديومي بكل لطف وراحة للطفل.
When will I receive the results, and can I discuss them with a specialist immediately?
The final report is issued within 21 working days; once released, you will receive a telephonic post‑ clinical guidance call to interpret the karyotype findings and discuss any follow‑up steps recommended by your neonatologist or pediatrician.
يصدر التقرير النهائي خلال 21 يوم عمل، وستتلقى بعدها مباشرة مكالمة استشارية هاتفية لشرح نتائج النمط النووي ومناقشة الخطوات التالية مع طبيب الأطفال المختص.
Legal & Regulatory Compliance: This service strictly adheres to Federal Decree‑Law No. 41 of 2024 (Article 87) on Patient Health Data Confidentiality, the UAE Child Data Sovereignty Law (2026) governing minor’s genetic information, and the UAE Personal Data Protection Law (PDPL). All analyses are performed under ISO 9001:2015 quality management system (Cert: INT/EGQ/2509DA/3139).
DHA Laboratory License No. 9834453. WhatsApp & support: +971 54 548 8731 (8 AM – 11 PM). Home collection available across all emirates.
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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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