Test Price
2,800 AED✅ Home Collection Available
KRT2 Gene (Ichthyosis, Bullous Type) Genetic Test in UAE | 2,800 AED | 2026 DHA Guidelines
تحليل جين KRT2 (السماك الفقاعي) باستخدام تقنية التسلسل الجيني من الجيل التالي في الإمارات | 2,800 درهم | معتمد من هيئة الصحة بدبي
Executive Summary
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO Accredited 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
- Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731
الملخص التنفيذي: يقدم هذا الاختبار الجيني الدقيق تحليلًا للطفرة في جين KRT2 المرتبط بالسماك الفقاعي، مع حساسية تشخيصية 99.9% بموجب معايير ISO 9001:2015، ويشمل خدمة سحب منزلي مع استشارة ما بعد الفحص.
Overview
The KRT2 Genetic Test sequences the entire keratin 2 gene to identify disease-causing variants responsible for epidermolytic ichthyosis (bullous type), a rare congenital blistering disorder. With a result turnaround of 3–4 weeks and a price of 2,800 AED, this assay delivers definitive molecular diagnosis for families seeking clarity and reproductive planning options.
| Feature | Our Test (KRT2 NGS Panel) | Closest Alternative (Whole Exome Sequencing) |
|---|---|---|
| Precision | Gene‑specific coverage with 99.9% analytical sensitivity for KRT2 | Broad exome coverage; incidental findings possible |
| Methodology | Next‑Generation Sequencing (NGS) with Sanger validation | Whole Exome Sequencing (WES) |
| Speed | 3–4 Weeks | 6–10 Weeks |
| Cost | 2,800 AED | 5,000–8,000 AED |
| Regulatory Compliance | DHA‑MOHAP approved; ISO 9001:2015 certified | Variable |
Physician Insight & Safety Protocol
Dr. PRABHAKAR REDDY (DHA: 61713011), Consultant Dermatologist, notes: “Witnessing the distress of neonatal blistering and fragile skin underscores the profound value of a definitive molecular diagnosis. This test, when integrated with clinical findings and a skin biopsy, empowers families with targeted management and genetic counselling. A negative result does not exclude other ichthyosis subtypes, so continuous dermatological follow‑up remains essential.”
Medication Warning
Do not discontinue prescribed medications (including retinoids) without consulting your doctor, as this may precipitate disease flares.
Exclusion Criteria & Emergency Red Flags
- Exclusion: Active life‑threatening sepsis, hemodynamic instability, or inability to provide a blood sample.
- Exclusion: Recent allogeneic stem cell transplant (may introduce donor DNA and confound germline analysis).
- Red Flag: Severe fluid loss from extensive blistering – risk of dehydration and electrolyte imbalance; seek urgent care.
- Red Flag: Signs of cutaneous infection (increased redness, pus, fever) requiring immediate medical attention.
Patient FAQ & Clinical Guidance
Q: What is the KRT2 gene test and what condition does it diagnose?
Snippet kill: The KRT2 NGS test detects pathogenic variants in the KRT2 gene responsible for epidermolytic ichthyosis (bullous type), allowing accurate diagnosis and family planning. It is used when a patient presents with blistering, erythroderma, and peeling skin at birth. A positive result confirms the genetic cause of bullous ichthyosis and helps predict severity and inheritance risks.
س: ما هو اختبار جين KRT2 وما الحالة التي يشخصها؟
يكشف اختبار KRT2 بالتسلسل الجيني عن الطفرات المسببة للسماك الفقاعي (انحلال البشرة الفقاعي) ويمكّن من التشخيص الدقيق وتخطيط الأسرة.
Q: How should I prepare for the test, and are any medications contraindicated?
Snippet kill: A simple blood draw, extracted DNA, or an FTA card with a few drops of blood is required, with no fasting needed. There is no medication contraindication for the genetic test itself; however, we strongly recommend a pre‑test genetic counselling session. Patients on retinoid therapy should continue their medication as prescribed and inform the clinician at the time of sample collection.
س: كيف أستعد للفحص وهل هناك أدوية ممنوعة؟
يُكتفى بعينة دم بسيطة أو بطاقة FTA، ولا يلزم الصيام. لا توجد أدوية ممنوعة للفحص الجيني، لكن ننصح بجلسة استشارة وراثية مسبقة.
Q: What is the turnaround time and price, and is insurance accepted?
Snippet kill: The test costs 2,800 AED and delivers results within 3–4 weeks, with direct insurance billing available via WhatsApp. Our ISO‑certified home collection service operates from 8 AM to 11 PM, and our team verifies coverage directly with your provider. You will also receive a post‑ teleconsultation to interpret the findings.
س: ما هي المدة والسعر وهل يُغطي التأمين تكلفة الفحص؟
السعر 2,800 درهم والنتائج خلال 3–4 أسابيع مع إمكانية الفوترة المباشرة للتأمين. يشمل الفحص خدمة السحب المنزلي واستشارة ما بعد النتيجة.
Legal & Regulatory Compliance:
This service adheres to Federal Decree‑Law No. 41 of 2024 (Art. 87), CDS Law 2026 (minor consent protocols), and the UAE Personal Data Protection Law (PDPL). Genetic data is processed strictly under confidentiality and never shared without explicit consent.
دعم ثنائي اللغة متاح
التحقق من التغطية التأمينية
Check Insurance Coverage Instantly
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