Test Price
2,800 AED✅ Home Collection Available
NSDHL Gene CK Syndrome Genetic Test in UAE | 2800 AED | 2026 DHA Guidelines
تحليل جين NSDHL لمتلازمة CK في الإمارات | 2800 درهم | معتمد من هيئة الصحة بدبي
Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO Accredited Processing. (ضمان الدقة: حساسية تشخيصية بنسبة 99.9% عبر معالجة معتمدة من ISO)
Premium Logistics: Paid Hospital-Grade Home Collection via ISO Certified Cold-Chain Home Collection and VIP Mobile Phlebotomy.
Clinical Guidance: Telephonic Post-Test Clinical Guidance in result interpretation.
Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731.
Overview
The NSDHL gene NGS test completely sequences the coding region for mutations causing CK syndrome, a rare X-linked neurological disorder characterized by intellectual disability and microcephaly. تحليل تسلسل الجين الكامل NSDHL بتقنية التسلسل من الجيل التالي يكشف الطفرات المسببة لمتلازمة CK النادرة بدقة عالية.
| Feature | Our NGS Test | Closest Alternative (Sanger Sequencing) |
|---|---|---|
| Diagnostic Precision | 99.9% sensitivity & specificity | ~99% sensitivity |
| Methodology | Next-Generation Sequencing (NGS) | Sanger Sequencing (single‑region focus) |
| Turnaround Time | 3 to 4 Weeks | 4 to 6 Weeks |
| Cost | 2800 AED | ~4000 AED |
Physician Insight & Safety Protocol
“As a neurologist, I understand the anxiety surrounding a possible genetic diagnosis like CK syndrome. This NGS test provides comprehensive data, but results must be interpreted within the full clinical picture and family history. I advise all patients and families to undergo pre- and post-test genetic counseling to fully understand implications.”
— Dr. PRABHAKAR REDDY, DHA License: 61713011
⚠ Do not discontinue prescribed medication without consulting your doctor.
Exclusion Criteria & Safety Red Flags
- Exclusion: Not recommended for individuals with active bleeding disorders or inability to provide a blood sample. For minors, a legal guardian must consent as per UAE CDS Law 2026.
- Emergency Red Flags: If you experience sudden seizure, loss of consciousness, or severe neurological deterioration, seek emergency medical attention immediately.
- This test is performed under UAE Federal Decree‑Law No. 41 of 2024, Art. 87, and complies with UAE PDPL data privacy regulations.
Patient FAQ & Clinical Guidance
What is CK syndrome and why is NSDHL gene testing important?
Snippet: CK syndrome is a rare X-linked intellectual disability disorder caused by mutations in the NSDHL gene, leading to microcephaly and neurological impairments.
متلازمة CK هي اضطراب نادر مرتبط بالكروموسوم X يسبب إعاقات ذهنية بسبب طفرات في جين NSDHL، مما يؤدي إلى صغر الرأس ومشاكل عصبية.
How is the test performed and what is the process?
Snippet: This genetic test analyses your blood DNA using advanced NGS technology to detect NSDHL mutations precisely.
يستخدم هذا الفحص الجيني عينة دم لتحليل الحمض النووي بتقنية NGS المتطورة لكشف طفرات NSDHL بدقة.
What support and guidance are provided after receiving results?
Snippet: Our post- clinical guidance provides a telephonic explanation of your NSDHL gene results by a specialist.
يقدم توجيهنا السريري بعد الفحص شرحًا هاتفيًا لنتائج جين NSDHL بواسطة أخصائي.
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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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All reports reviewed by DHA-Certified physicians