Test Price
2,800 AED✅ Home Collection Available
CDK6 Gene Microcephaly, Autosomal Recessive Type 12 Genetic Test in UAE | 2800 AED | 2026 DHA Guidelines
تحليل جين CDK6 لصغر الرأس الصبغي الجسدي المتنحي من النوع 12 بتقنية التسلسل من الجيل التالي في الإمارات | 2800 درهم | معتمد من هيئة الصحة بدبي
الموثوقية والامتثال الإكلينيكي
عند إجراء تحليل جين CDK6 في مختبرنا المعتمد من هيئة الصحة بدبي، نضمن دقة تشخيصية تصل إلى 99.9% عبر تقنية التسلسل من الجيل التالي (NGS) بموجب شهادة ISO 9001:2015.
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 Certified NGS Processing.
- Premium Logistics: Paid Hospital-Grade Home Collection via ISO Certified Cold-Chain Home Collection & VIP Mobile Phlebotomy.
- Clinical Guidance: Telephonic Post-Test Clinical Guidance in result interpretation by DHA-licensed genetic counselors.
- Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731.
Overview
The CDK6 Gene Microcephaly NGS Test identifies pathogenic mutations in the CDK6 gene, which cause autosomal recessive primary microcephaly type 12, a severe neurodevelopmental disorder. يساعد هذا التحليل الجيني الدقيق في تشخيص صغر الرأس الوراثي وتحديد الحاملين للمرض، مما يمكّن من التخطيط العائلي المستنير.
| Feature | Our CDK6 NGS Test | Standard PCR/Sanger Panel |
|---|---|---|
| Precision | Full gene coverage with 99.9% analytical sensitivity | Hotspot analysis only; risk of missing novel variants |
| Methodology | Illumina NovaSeq X Plus NGS, Sanger validation | Capillary Sanger sequencing of targeted exons |
| Turnaround Time | 3 to 4 Weeks | 6 to 8 Weeks |
| Regulatory Standard | DHA/MOHAP 2026, ISO 9001:2015 | Variable laboratory certifications |
Physician Insight & Safety Protocol
“While this test provides definitive genetic confirmation of CDK6-related microcephaly, a negative result does not rule out other genetic or environmental causes; therefore, comprehensive clinical evaluation remains essential. I advise all patients to review results with a pediatric neurologist and certified genetic counselor, because the same mutation can exhibit variable expressivity. This test is a powerful tool, but it must be integrated with thorough physical examination and family history.”
— Dr. PRABHAKAR REDDY (DHA License: 61713011), Consultant Clinical Geneticist
⚠️ Medication Warning: Do not discontinue prescribed medication without consulting your doctor.
Exclusion Criteria & ER Red Flags
- Exclusion Criteria: Active systemic infection or hemodynamic instability precluding safe venipuncture; inability to provide informed consent; testing of minors without legal guardian consent (per UAE CDS Law 2026).
- Emergency Red Flags: New‑onset seizures, acute loss of developmental milestones, signs of raised intracranial pressure (projectile vomiting, lethargy, bulging fontanelle), or sudden neurological regression. Seek immediate emergency medical attention.
- Data Privacy: All genetic data are protected under UAE PDPL (Federal Decree‑Law No. 45 of 2021) and stored exclusively on HIPAA‑compliant servers within the UAE.
- Legal Mandate: This test is provided in full accordance with Federal Decree‑Law No. 41 of 2024 (Article 87) regarding genetic testing oversight, and the 2026 Child Digital Safety (CDS) Law for minors.
Patient FAQ & Clinical Guidance
1. What is the CDK6 gene test used for?
Diagnostic Precision: This test sequences the entire CDK6 gene to diagnose autosomal recessive primary microcephaly type 12, confirm carrier status, and guide family planning. يُستخدم هذا الفحص لتشخيص صغر الرأس الأولي من النوع 12 وتحديد الحاملين للطفرة الجينية وتوجيه الاستشارة الوراثية.
2. What sample types are accepted, and how is the collection arranged?
Convenience & Options: We accept whole blood, extracted DNA, or a single drop of blood on an FTA card; our premium home collection service ensures cold‑chain transport across all emirates. نقبل عينات الدم الكامل، الحمض النووي المستخلص، أو قطرة دم واحدة على بطاقة FTA، مع خدمة سحب منزلي متميزة.
3. How should I prepare for the test, and is genetic counseling required?
Optimal Preparation: A pre‑ genetic counseling session is mandatory to draw a detailed family pedigree and discuss implications; no fasting is needed unless combined with other bloodwork. الجلسة الاستشارية الوراثية قبل الفحص إلزامية لرسم شجرة العائلة ومناقشة النتائج المحتملة.
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