Test Price
2,800 AED✅ Home Collection Available
CYP4F22 Gene Ichthyosis, Lamellar Type 3 Genetic Test in UAE | 2800 AED | 2026 DHA Guidelines
تحليل جين CYP4F22 لمرض السُماك الصفائحي من النوع الثالث في الإمارات | 2800 درهم | معتمد من هيئة الصحة بدبي
نضمن دقة تشخيصية تصل إلى 99.9% باستخدام أحدث تقنيات التسلسل الجيني (NGS) في مختبرات معتمدة من ISO، مع خدمة سحب عينات منزلية فائقة الجودة وتفسير طبي هاتفي بعد النتيجة.
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 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.
Comprehensive Genetic Assessment for Lamellar Ichthyosis Type 3
The CYP4F22 gene NGS test detects pathogenic variants responsible for autosomal recessive lamellar ichthyosis type 3, offering a definitive molecular diagnosis for affected individuals and their families. يُتيح تحليل جين CYP4F22 تشخيصًا جينيًا دقيقًا للسُماك الصفائحي من النوع الثالث، مما يساعد العائلات في الإمارات على فهم المخاطر الوراثية واتخاذ قرارات مستنيرة.
| Feature | Our NGS Test (Full Gene) | Closest Alternative (Sanger Sequencing) |
|---|---|---|
| Precision | 99.9% sensitivity for all coding regions & splice sites | Limited to pre‑selected exons; may miss 20% of variants |
| Method | Next‑Generation Sequencing (NGS) with orthogonal confirmation | Conventional Sanger sequencing |
| Speed | 3‑4 Weeks | 6‑8 Weeks |
| Price | 2800 AED | ~2500 AED (partial coverage) |
Clinical Interpretation & Safety Mandates
“Every lamellar ichthyosis case carries unique genetic nuances; a positive CYP4F22 result must be correlated with phenotypic findings and family history to guide personalised management. I emphasize that patients should not make treatment changes solely based on this report without in‑person clinical evaluation. Your health journey deserves a multidisciplinary approach that includes dermatology, genetics, and supportive care.”
— Dr. PRABHAKAR REDDY, DHA License: 61713011
Medication Warning: Do not discontinue prescribed medication or alter therapy without consulting your doctor.
Patient Safety – Exclusion Criteria & Red Flags
- Exclusion: Infants under 3 months (alternative buccal swab recommended); active systemic infection or fever >38.5°C requires postponement.
- Exclusion: Known severe coagulopathy or platelet disorder (e.g., haemophilia A/B) without prior haematologist clearance for venipuncture.
- ER Red Flags: If you experience acute skin blistering, widespread erosions, or signs of secondary infection (pus, fever) after sample collection, seek immediate emergency care.
- Emergency Contact: For medical emergencies, dial 998 (UAE Ambulance) or visit the nearest hospital emergency department.
Frequently Asked Questions
What does the CYP4F22 gene test detect?
The CYP4F22 NGS test identifies pathogenic DNA variants in the entire coding region of the CYP4F22 gene responsible for lamellar ichthyosis type 3, confirming a molecular diagnosis in as little as 3 weeks.
يكشف تحليل CYP4F22 عن الطفرات المسببة للسُماك الصفائحي من النوع الثالث، مما يسمح بتأكيد التشخيص وتقدير المخاطر الوراثية لدى أفراد العائلة الإماراتية.
How should I prepare for the test?
A pre‑ genetic counselling session is required to draw a family pedigree and collect clinical history; no fasting is necessary, but you must inform the phlebotomist of any anticoagulant use.
يلزم استشارة وراثية قبل الفحص لرسم شجرة العائلة وتوثيق التاريخ السريري، كما يجب إبلاغ الفني عن أي أدوية مميعة للدم قبل سحب العينة.
Is home collection available and safe for children?
Yes, our VIP paediatric phlebotomy service includes ISO‑certified cold‑chain transport from your home (8 AM–11 PM) ensuring sample integrity and minimal distress for your child.
نقدم خدمة سحب العينات المنزلية للأطفال مع فريق تمريض متخصص ونقل مبرد معتمد من ISO، مما يضمن راحة طفلك وسلامة العينة من منزلكم في الإمارات.
UAE Legal & Quality Compliance:
This laboratory service adheres to Federal Decree‑Law No. 41 of 2024 (Art. 87), the 2026 CDS Law (Minors protection), and UAE Personal Data Protection Law (PDPL) for genetic information confidentiality.
ISO 9001:2015 Certified – Cert. INT/EGQ/2509DA/3139. Genetic counselling and testing are supervised by DHA‑licensed medical professionals.
Support & WhatsApp: +971 54 548 8731 | Facility License: 9834453
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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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