Test Price
2,800 AED✅ Home Collection Available
CLCF1 Gene Cold-Induced Sweating Syndrome Type 2 Genetic Test in UAE | 2800 AED | 2026 DHA Guidelines
تحليل الجين CLCF1 لمتلازمة التعرق الناتج عن البرد من النوع الثاني في الإمارات | 2800 درهم | معتمد من هيئة الصحة بدبي
Executive Summary الملخص التنفيذي
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity for targeted CLCF1 gene via ISO‑accredited NGS.
دقة تشخيصية 99.9% لجين CLCF1 باستخدام تقنية الجيل التالي (NGS) المعتمدة. - Premium Logistics: Paid Hospital‑Grade Home Collection with ISO Certified Cold‑Chain Transport & VIP Mobile Phlebotomy (8 AM‑11 PM).
خدمة سحب منزلي بالمستشفى معتمدة بنقل مبرد حسب الأيزو وخدمة سحب الدم المتنقلة المميزة. - Clinical Guidance: Post‑Test Telephonic Clinical Guidance for result interpretation by genetics specialists.
استشارة هاتفية بعد الفحص لتفسير النتائج مع أخصائيي الوراثة. - Insurance: Direct Billing Verification via WhatsApp at +971 54 548 8731.
التحقق المباشر من تغطية التأمين عبر واتساب على الرقم +971 54 548 8731.
Overview
The CLCF1 Genetic Test identifies pathogenic variants in the CLCF1 gene responsible for Cold‑Induced Sweating Syndrome Type 2, a rare autosomal recessive disorder. This test supports early diagnosis, personalised clinical management, and accurate genetic counselling for affected families.
يكشف هذا الاختبار عن الطفرات المرضية في جين CLCF1 المرتبطة بمتلازمة التعرق الناتج عن البرد من النوع الثاني، مما يساعد في التشخيص المبكر والتوجيه الوراثي للعائلات.
| Feature | Our CLCF1 NGS Gene Test (DHA‑Approved) | Whole Exome Sequencing (WES) Alternative |
|---|---|---|
| Gene Coverage | Full CLCF1 gene (exons, intron‑exon boundaries, deep intronic regions) | All ~20,000 genes; may miss deep intronic variants or require reflex testing |
| Analytical Sensitivity | ≥99.9% for targeted region | Variable; often needs Sanger validation |
| Turnaround Time | 3–4 Weeks | 6–12 Weeks |
| Price | 2800 AED | 5,000–8,000 AED |
| Incidental Findings | None (gene‑specific) | Possible, requiring complex counselling |
| Home Collection | Included, cold‑chain | Often limited or extra charge |
Physician Insight & Safety Protocol
🧬 Dr. Prabhakar Reddy (DHA License No. 61713011):
“Cold‑Induced Sweating Syndrome is a rare, often under‑recognised condition. This NGS test is a powerful tool, yet a thorough clinical evaluation—including family history and physical findings—remains essential. I encourage all families to discuss the results with a paediatrician or clinical geneticist before making any health decision. The test is not a standalone diagnosis; it is one piece of a broader clinical puzzle.”
⛔ Medication Warning: Do not discontinue any prescribed medication without consulting your doctor.
Safety: Exclusion Criteria & ER Red Flags
- Exclusion Criteria: Individuals without clinical suspicion of CISS2 or without a documented family history should not undergo this targeted test without prior genetic counselling. Testing of minors must comply with UAE CDS Law 2026 – only a legal guardian can provide informed consent.
- Emergency Red Flags: If you or your child experience severe sweating episodes accompanied by hypothermia (core temperature <35 °C), breathing difficulties, or altered consciousness, seek emergency medical attention immediately.
Patient FAQ & Clinical Guidance
1. What is the CLCF1 gene test used for?
The CLCF1 Genetic Test identifies pathogenic mutations in the CLCF1 gene causing Cold‑Induced Sweating Syndrome Type 2, a rare disorder characterised by cold‑induced sweating, craniofacial abnormalities, and skeletal issues. Detection of biallelic variants confirms the diagnosis, enables reproductive planning, and guides symptom‑specific monitoring such as orthopaedic and respiratory follow‑up.
يُستخدم اختبار جين CLCF1 لتحديد الطفرات المسببة لمتلازمة التعرق الناتج عن البرد من النوع الثاني، وهو مرض وراثي نادر يؤدي إلى تعرق بارد وتشوهات هيكلية.
2. How is the sample collected and what is the turnaround time?
A blood sample or a single drop of blood on an FTA card is collected at your home by a certified phlebotomist, and results are delivered in 3 to 4 weeks. The sample is transported under strict cold‑chain conditions to our ISO‑certified laboratory. You can choose between whole blood, extracted DNA, or dried blood spot (FTA card) options depending on your convenience and clinical scenario.
يتم جمع عينة دم أو قطرة دم واحدة على بطاقة FTA في المنزل عن طريق أخصائي سحب دم معتمد، وتُصدر النتائج خلال 3 إلى 4 أسابيع.
3. Is this covered by insurance in the UAE?
Insurance coverage for genetic testing varies; we provide direct billing verification via WhatsApp at +971 54 548 8731 to check your specific policy. Many UAE insurers require pre‑authorisation and a referral from a paediatrician or clinical geneticist. Our team assists with the required documentation to maximise your reimbursement chance.
تختلف تغطية التأمين للفحوصات الجينية؛ نوفر خدمة التحقق المباشر من التغطية عبر واتساب على الرقم +971 54 548 8731.
✔ Compliant with Federal Decree‑Law No. 41 of 2024 (Art. 87), UAE CDS Law 2026 (Minors), and UAE PDPL.
✔ Facility License No. 9834453 · ISO 9001:2015 Certification: 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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All reports reviewed by DHA-Certified physicians