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2,800 AED

✅ Home Collection Available

WNT5A Gene (Robinow Syndrome, Autosomal Dominant Type 1) Genetic Test in UAE | 2800 AED | 2026 DHA Guidelines

تحليل جين WNT5A (متلازمة روبينو السائدة من النوع 1) في الإمارات | 2800 درهم | إرشادات هيئة الصحة بدبي 2026

ملخص تنفيذي: تشخيص جيني فائق الدقة لمتلازمة روبينو السائدة عبر تقنية التسلسل الجيني من الجيل التالي، مطابق لأحدث معايير هيئة الصحة بدبي ومنظمة الصحة العالمية.

  • Clinical Accuracy: 99.9% Diagnostic Sensitivity for coding exons and canonical splice sites via ISO 9001:2015 Accredited Processing.
  • Premium Logistics: Paid Hospital-Grade Home Collection (8 AM – 11 PM) with ISO Certified Cold-Chain Transport and VIP Mobile Phlebotomy.
  • Clinical Guidance: Telephonic Post-Test Clinical Interpretation support by DHA-licensed genetic specialists.
  • Insurance & Billing: Direct Electronic Billing Verification via WhatsApp at +971 54 548 8731.

Overview – WNT5A Gene NGS Test for Robinow Syndrome

This targeted Next Generation Sequencing (NGS) assay analyzes the entire coding region of the WNT5A gene, identifying pathogenic variants responsible for autosomal dominant Robinow syndrome (ADRS) with >99.9% analytical sensitivity. يستخدم الاختبار تقنية التسلسل الجيني من الجيل التالي لفحص الجين الكامل وتأكيد التشخيص بدقة عالية. Results guide precise clinical management, genetic counseling, and family risk assessment.

ParameterOur WNT5A NGS TestClosest Alternative (Sanger Sequencing)
Precision99.9% detection of SNVs, indels in coding exons ±10 bp~95% due to limited coverage of GC-rich regions
MethodHigh-depth NGS with orthogonal confirmationCapillary electrophoresis – slower, single variant focus
Turnaround Time3–4 Weeks (expedited options available)4–6 Weeks, often batched

Physician Insight & Safety Protocol

“As a clinical geneticist, I emphasize that a negative result does not rule out other dysmorphic syndromes; always correlate with full physical examination and family pedigree. A positive result enables early intervention, but decisions should never be based on this test alone. I strongly advise pre- and post-test genetic counseling for every family.” — Dr. PRABHAKAR REDDY, DHA License: 61713011

⚠ Do not discontinue or modify any prescribed medication without consulting your treating physician.

Exclusion Criteria & Emergency Red Flags

  • Receipt of allogeneic blood transfusion, bone marrow/stem cell transplant, or leukoreduced products within the last 4 weeks (risk of donor DNA contamination).
  • Uncertain paternity or undisclosed donor conception must be declared for accurate interpretation.
  • Patients under 18 require documented parental/guardian consent in compliance with UAE CDS Law 2026.
  • ER Red Flags: Seek immediate emergency care if the child develops acute respiratory distress, cyanosis, severe feeding difficulties, or sudden neurological deterioration—these may require urgent intervention beyond the test scope.

Patient FAQ & Clinical Guidance

How accurate is the WNT5A genetic test for confirming Robinow syndrome diagnosis?

The test delivers >99.9% analytical sensitivity and specificity for pathogenic single nucleotide and indel variants, confirming diagnosis with near-perfect reliability. يقدم الاختبار حساسية ونوعية تحليلية تزيد عن 99.9% للطفرات المرضية مما يؤكد التشخيص بشكل شبه مؤكد.

What information must I bring for the pre-test genetic counseling session?

You will need a detailed three-generation family pedigree, clinical photographs of affected members, and any previous ultrasound or dysmorphology reports to maximize test interpretation accuracy. يجب إحضار تاريخ عائلي مفصل لثلاثة أجيال، صور طبية، وتقارير سابقة لتحقيق أقصى دقة في التفسير الجيني.

Can the be performed if the patient is a newborn or infant under UAE law?

Yes, with mandatory prior genetic counseling, signed parental consent as per CDS Law 2026, and a clinical indication; the blood sample can be safely collected from an infant’s heel or venipuncture. نعم، بشرط استيفاء موافقة الوالدين وجلسة استشارة وراثية وفقاً للقانون الاتحادي رقم 41 لسنة 2024 وتشريعات حماية القاصرين.

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