Test Price
2,800 AED✅ Home Collection Available
PARN Gene Dyskeratosis Congenita (Autosomal Recessive Type 6) Genetic Test in UAE | AED 2800 | 2026 DHA Guidelines
تحليل جين PARN لخلل التقرن الخلقي (النوع السادس الصبغي الجسدي المتنحي) بتقنية التسلسل الجيني الجديد في الإمارات | 2800 درهم | معتمد من هيئة الصحة بدبي
Executive Summary
- ✓ 99.9% Diagnostic Sensitivity via ISO Accredited Processing.
دقة تشخيصية 99.9% عبر معالجة معتمدة بمواصفة ISO. - ✓ Premium Logistics: Hospital‑Grade Home Collection with ISO‑Certified Cold‑Chain & VIP Mobile Phlebotomy.
خدمة سحب منزلية مبردة ومعتمدة بتقنية VIP للسلامة. - ✓ Clinical Guidance: Telephonic Post‑Test Clinical Result Interpretation.
استشارة سريرية هاتفية بعد صدور النتيجة. - ✓ Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731.
التحقق من تغطية التأمين مباشرة عبر واتساب.
Overview
The PARN gene NGS test identifies pathogenic variants responsible for Dyskeratosis Congenita autosomal recessive type 6, a rare inherited disorder affecting skin, nails, and bone marrow. This comprehensive analysis delivers precise mutation detection, guiding clinical management and family planning. يكشف تحليل جين PARN الطفرات المسببة لخلل التقرن الخلقي، مما يوجه العلاج والتخطيط العائلي.
| Feature | Our Test (PARN NGS) | Closest Alternative (Sanger) |
|---|---|---|
| Methodology | Next‑Generation Sequencing (NGS) | Sanger Sequencing |
| Coverage | Full PARN gene (all exons & splice sites) | Limited to known hotspots |
| Turnaround Time | 3–4 Weeks | 5–6 Weeks |
| Cost | AED 2800 | AED 2500 (less comprehensive) |
Physician Insight & Safety Protocol
“As a clinical pathologist, I affirm that NGS‑based PARN gene testing offers exceptional sensitivity, yet results must always be correlated with clinical findings and family history. A negative result does not eliminate the need for lifelong surveillance for dyskeratosis congenita complications. Please do not change any treatment without consulting your supervising physician.”
— Dr. Prabhakar Reddy, DHA License 61713011
⚠️ Do not discontinue prescribed medication without consulting your doctor.
Safety Exclusion Criteria & Emergency Red Flags
- Not a general wellness screen – requires clinical indication and a specialist referral.
- Mandatory pre‑test genetic counselling session and pedigree charting.
- Unsuitable for asymptomatic individuals without family history or professional guidance.
- ER Alert: Seek immediate medical help if you experience sudden severe bleeding, spontaneous bruising, extreme fatigue, recurrent infections, or pallor (signs of bone marrow failure).
Patient FAQ & Clinical Guidance
1. What is Dyskeratosis Congenita and how does the PARN gene test help?
The PARN gene test identifies mutations causing dyskeratosis congenita type 6, a rare inherited bone marrow failure syndrome with skin and nail abnormalities. It allows early diagnosis, targeted surveillance for cancer and pulmonary fibrosis, and informed reproductive counseling. يحدد تحليل جين PARN الطفرات المسببة لخلل التقرن الخلقي، مما يتيح التشخيص المبكر والمتابعة الدقيقة.
2. How is the performed and what is the turnaround time?
A simple blood draw, extracted DNA, or a single drop on an FTA card is collected and analyzed using next-generation sequencing; results are ready within 3 to 4 weeks. Home collection service is available from 8 AM to 11 PM daily. يتم جمع العينة عبر سحب دم بسيط أو بطاقة FTA، وتظهر النتائج بعد 3 إلى 4 أسابيع مع خدمة السحب المنزلي.
3. Is home collection available and what is the cost?
Yes, VIP home phlebotomy by DHA‑licensed professionals is offered nationwide (8 AM – 11 PM) for AED 2800, with direct insurance billing verification via WhatsApp at +971 54 548 8731. نعم، تتوفر خدمة السحب المنزلي VIP مقابل 2800 درهم مع إمكانية التأمين المباشر عبر واتساب.
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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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