Test Price
2,800 AED✅ Home Collection Available
CDKN1C Gene IMAGE Syndrome Genetic Test in UAE | 2800 AED | 2026 DHA Guidelines
تحليل جين CDKN1C لمتلازمة IMAGE في الإمارات | 2800 درهم | معتمد من هيئة الصحة بدبي
Executive Summary – ملخص تنفيذي
Diagnostic Certainty: 99.9% analytical sensitivity for CDKN1C gene variants via ISO 9001:2015-accredited next‑generation sequencing (NGS) – the gold standard for IMAGE syndrome confirmation in the UAE. Premium Logistics: Hospital‑grade home collection (08:00 – 23:00), VIP mobile phlebotomy, and ISO‑certified cold‑chain transport. Clinical Guidance: Complimentary tele‑post‑test interpretation anchored in DHA/MOHAP protocols. Insurance: Direct billing verification via WhatsApp +971 54 548 8731.
اختبار دقيق للغاية لتسلسل جين CDKN1C يساعد في تشخيص متلازمة IMAGE النادرة. يتم التحليل باستخدام تقنية NGS المعتمدة وفق معايير ISO 9001:2015، مع إمكانية الجمع المنزلي والاستشارة الطبية بعد النتيجة.
Test Overview & Clinical Positioning
This single‑gene NGS test fully sequences the CDKN1C gene to detect pathogenic variants underlying IMAGE syndrome (intrauterine growth restriction, metaphyseal dysplasia, adrenal hypoplasia, and genital anomalies). Designed for pediatric and neonatal dysmorphology work‑ups, it delivers actionable molecular data within 3–4 weeks.
| Feature | Our NGS CDKN1C Test | Standard Sanger Sequencing |
|---|---|---|
| Gene Coverage | Full coding region ±20 bp exon‑intron boundaries | Limited to pre‑selected exonic segments |
| Analytical Sensitivity | 99.9% (pathogenic/likely pathogenic CNV & SNVs) | ~95% for targeted SNPs only |
| Turnaround Time | 3–4 weeks | 6–8 weeks |
| Clinical Utility | Comprehensive dysmorphology diagnosis & family counselling | Variant‑specific follow‑up only |
Physician Insight & Safety Protocol
“As a clinical geneticist, I advise that every CDKN1C result must be integrated with your child’s full clinical picture by a pediatric specialist. This test reveals a predisposition; it never replaces the nuanced judgment of a dysmorphology expert. Please continue all prescribed treatments unless directed otherwise by your physician.”
— Dr. PRABHAKAR REDDY, DHA License No. 61713011
CRITICAL MEDICATION NOTICE
Do not discontinue prescribed medication without consulting your doctor. Sudden withdrawal of corticosteroid therapy in adrenal insufficiency can be life‑threatening.
Exclusion Criteria & Emergency Red Flags
- Hemodynamically unstable infants unable to tolerate venipuncture
- Active infection at the phlebotomy site
- Contraindicated genetic testing for minors without legal guardian consent (CDS Law 2026)
- Seek ER care immediately if: signs of adrenal crisis (vomiting, severe dehydration, hypotension, altered consciousness) develop in an undiagnosed neonate
Patient FAQ & Clinical Guidance
Q1: What is the CDKN1C IMAGE Syndrome Genetic Test?
ما هو اختبار الجين CDKN1C للتسلسل الجيني لمتلازمة IMAGE؟
This next‑generation sequencing test analyzes the entire CDKN1C gene to identify pathogenic variants causing IMAGE syndrome, a rare disorder marked by prenatal growth failure, skeletal dysplasia, adrenal hypoplasia, and genital anomalies. The result guides precise management, hormone replacement, and genetic counseling for families across the UAE. Processing follows DHA‑endorsed NGS protocols under ISO 9001:2015 certification (Cert: INT/EGQ/2509DA/3139). يحدد هذا الفحص الطفرات المسببة لمتلازمة IMAGE ليساعد في التشخيص المبكر والعلاج الهرموني المناسب.
Q2: How is the sample collected for CDKN1C testing in the UAE?
كيف تُجمع العينة لفحص جين CDKN1C في الإمارات؟
A certified pediatric phlebotomist performs a gentle home blood draw or collects an FTA card blood spot, using infant‑friendly techniques to minimize discomfort while maintaining specimen integrity. We accept whole blood, extracted DNA, or a single drop on an FTA card. Samples are transported under cold‑chain logistics (ISO validated) directly to our CAP‑accredited molecular lab. The entire process is coordinated via WhatsApp +971545488731 and complies with UAE PDPL data privacy requirements. يتم جمع العينة بواسطة ممرض معتمد في المنزل باستخدام تقنيات مناسبة للرضع، مع نقل مبرد وفق القوانين الإماراتية لحماية البيانات.
Q3: What are the turnaround time and price for full CDKN1C gene sequencing?
ما المدة المطلوبة وتكلفة تسلسل جين CDKN1C الكامل؟
Results are delivered within 3 to 4 weeks at a fixed cost of 2,800 AED, including comprehensive variant interpretation, a clinician‑friendly report, and a post‑ tele‑consultation with our genetic team. This price covers the entire analytical pipeline from library preparation to bioinformatic annotation using ClinVar, gnomAD, and DHA‑curated variant databases. Direct insurance billing can be verified instantly via WhatsApp. تظهر النتائج خلال 3–4 أسابيع بتكلفة 2800 درهم شامل التفسير السريري والاستشارة الطبية الهاتفية بعد الاختبار.
UAE Healthcare Compliance & Accreditation
- Federal Decree‑Law No. 41 of 2024 on Medical Liability (Art. 87) – all risks disclosed
- CDS Law 2026 – strict minor consent and data safeguards adhered to
- UAE Personal Data Protection Law (PDPL) – genomic data encrypted and stored locally
- Facility License: 9834453 | ISO 9001:2015 certified (Cert: INT/EGQ/2509DA/3139)
دعم ثنائي اللغة متاح
التحقق من التغطية التأمينية
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Stop the guesswork. Send a photo of your Insurance Card and Doctor's Prescription to our DHA-Certified Verification Team on WhatsApp.
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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