Test Price
2,800 AED✅ Home Collection Available
ST14 Gene Genetic Test for Autosomal Recessive Congenital Ichthyosis Type 11 (ARCI11) in UAE | 2800 AED | 2026 DHA Guidelines
تحليل جين ST14 للسمكية الخلقية الصبغية المتنحية من النوع 11 (ARCI11) في الإمارات | 2800 درهم | إرشادات هيئة الصحة بدبي 2026
Executive Summary: The ST14 Gene NGS Test delivers 99.9% diagnostic sensitivity for autosomal recessive congenital ichthyosis type 11 (ARCI11), processed in our ISO 9001:2015 certified laboratory. Benefit from hospital-grade home collection across the UAE via cold-chain logistics, VIP mobile phlebotomy (8 AM–11 PM), and post-test clinical guidance. We handle direct billing verification with all major insurers—simply share your card via WhatsApp +971 54 548 8731. الفحص الجيني للجين ST14 يقدم دقة تشخيصية تصل إلى 99.9% مع خدمة سحب منزلي متميزة واستشارة طبية بعد النتيجة؛ نرافقك بكل خطوة وفق أحدث معايير هيئة الصحة بدبي.
Clinical Overview
This targeted Next-Generation Sequencing (NGS) assay analyses all coding exons and splice junctions of the ST14 gene, the definitive marker for autosomal recessive congenital ichthyosis type 11 (ARCI11). It replaces older single-gene Sanger workflows with a highly multiplexed, LC‑MS/MS‑validated sequencing chemistry that ensures complete exon coverage and variant detection even in challenging GC‑rich regions. يكشف التحليل عن الطفرات المسببة للسمكية الخلقية المتنحية المرتبطة بجين ST14، ويستخدم تقنية متطورة لتحديد التغيرات الجينية بدقة فائقة.
| Feature | Our Test (ST14 NGS) | Closest Alternative (Single‑Gene Sanger) |
|---|---|---|
| Diagnostic Precision | 99.9% analytical sensitivity, full gene coverage | ~98% per amplicon; may miss deep intronic variants |
| Methodology | NGS with Illumina® platform, bioinformatic variant calling | Sanger sequencing, limited to defined regions |
| Turnaround Time | 3 to 4 weeks | 6 to 8 weeks |
| UAE Compliance | DHA/MOHAP registered, ISO 9001:2015, PDPL-compliant | Variable; rarely ISO certified |
Physician Insight & Safety Protocol
“The ST14 NGS test provides a cornerstone for the precise molecular diagnosis of ARCI11. While results are highly accurate, they must always be correlated with clinical findings and family history. I encourage every patient to undergo a structured genetic counselling session before and after the test to interpret the implications fully.”
— Dr. PRABHAKAR REDDY, DHA License: 61713011, Consultant in Genomic Medicine
Do not discontinue or adjust any prescribed topical or systemic medication (retinoids, emollients, keratolytics) without explicit instruction from your consultant dermatologist or paediatrician.
Exclusion Criteria & Red Flags
- Acute febrile illness or active systemic infection at time of sample collection.
- Recent whole blood transfusion (< 4 weeks) or bone marrow transplant.
- Lack of informed consent or refusal of mandatory pre‑test genetic counselling session.
- If the patient exhibits severe erythema, blistering, or signs of neonatal sepsis, seek immediate emergency care—do not delay for genetic testing.
- Failure to thrive, electrolyte imbalances, or respiratory distress in a newborn requires urgent paediatric assessment.
Patient FAQ & Clinical Guidance
1. What exactly does the ST14 NGS test detect, and how accurate is it?
ما الذي يكشفه فحص جين ST14 بالتحديد وما مدى دقته؟
The ST14 NGS identifies single nucleotide variants, small insertions/deletions, and copy number changes in all coding exons of the ST14 gene with 99.9% analytical sensitivity. It is the most comprehensive molecular assay for ARCI11, validated on hundreds of clinical samples in our DHA‑licensed facility. Results are interpreted according to ACMG/AMP guidelines, and every report includes a clinician‑friendly pathogenicity classification.
2. Is home collection available across all UAE emirates and how should I prepare?
هل تتوفر خدمة السحب المنزلي في جميع الإمارات وكيف أستعد؟
Our ISO‑certified cold‑chain mobile phlebotomy team reaches Abu Dhabi, Dubai, Sharjah, Ajman, Umm Al Quwain, Ras Al Khaimah, and Fujairah daily from 8 AM to 11 PM. No fasting is required; simply continue your regular medication and skincare routine. A trained phlebotomist collects a single 3 mL EDTA whole blood or a dried blood spot on an FTA card, ensuring sample stability during transport.
3. How long until I receive my report and what support do you offer afterwards?
متى تظهر النتيجة وما نوع الدعم المتاح بعد الفحص؟
The final signed report is delivered within 3 to 4 weeks via encrypted email and patient portal. Once results are ready, you may schedule a complimentary 15‑minute telephonic clinical guidance session with Dr. Reddy’s team to interpret the findings, understand recurrence risks, and plan any necessary dermatological or paediatric follow‑up.
DNA Health & Wellness Lab
Facility License: 9834453 | ISO 9001:2015 (Cert: INT/EGQ/2509DA/3139)
Certified by Dubai Health Authority (DHA) and Ministry of Health and Prevention (MOHAP)
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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