Test Price
2,800 AED✅ Home Collection Available
HR Gene Atrichia with Papular Lesions Genetic Test in UAE | 2800 AED | 2026 DHA Guidelines
تحليل جين HR (انعدام الشعر مع حطاطات) في الإمارات | 2800 درهم | معتمد من هيئة الصحة بدبي
الملخص التنفيذي
- ✔ ضمان الدقة: قدرة تشخيصية 99.9% باستخدام تسلسل الجيل التالي (NGS) المعتمد وفق معايير ISO 9001:2015.
- ✔ خدمات لوجستية متميزة: خدمة سحب الدم المنزلي عبر سلسلة تبريد معتمدة (VIP Mobile Phlebotomy) مع خيار بطاقة FTA، تعمل من 8 صباحاً حتى 11 مساءً.
- ✔ توجيه سريري: استشارة هاتفية بعد الاختبار لتفسير النتائج من مختصين معتمدين.
- ✔ التحقق من التأمين: التحقق المباشر من التغطية التأمينية عبر واتساب على الرقم 971545488731+.
Overview
The HR Gene Atrichia with Papular Lesions Genetic Test definitively identifies pathogenic variants in the HR gene, the sole known cause of this rare autosomal recessive hair loss disorder, using next‑generation sequencing with 99.9% analytical sensitivity. Our DHA‑accredited UAE laboratory delivers actionable, physician‑interpreted results within 3–4 weeks from blood, extracted DNA, or a simple finger‑prick FTA card, empowering personalized clinical decision‑making and family planning.
| Feature | Our Test (HR Gene NGS) | Closest Alternative (Whole Exome Sequencing) |
|---|---|---|
| Precision | Targeted HR gene with Sanger confirmation – 99.9% sensitivity | Broad coverage; variants of uncertain significance common |
| Methodology | NGS + bidirectional Sanger sequencing | NGS only |
| Turnaround | 3–4 weeks | 6–12 weeks |
| Cost (UAE) | 2800 AED | ~4500–6000 AED |
| DHA Accreditation | Yes (License 9834453) | Variable |
Physician Insight & Safety Protocol
“As a dermatologist with DHA license 61713011, Dr. PRABHAKAR REDDY emphasizes that this genetic test is a powerful diagnostic tool but must be correlated with clinical findings and family history. A confirmed HR mutation not only explains the lifelong hair loss but also guides prognosis, genetic counseling, and potential future therapeutic avenues. However, a negative test does not completely exclude other rare genodermatoses, and clinical follow‑up remains essential.”
⚠️ Medication Warning: Do not discontinue prescribed medication without consulting your doctor. This test does not replace clinical management.
Safety & Exclusion Criteria
- Exclusion criteria: Pediatric patients with severe anemia, active infection, or bleeding disorders may require modified collection; pre‑test assessment is mandatory.
- Emergency Red Flags: If this test is requested for a minor under CDS Law 2026, explicit guardian consent and a child‑safeguarding assessment are mandatory. Any suspicion of non‑accidental injury must be reported immediately to UAE child protection authorities.
- Test limitations: Only the HR gene is analyzed; other hair‑loss genes are not included. Results must be interpreted by a qualified clinical geneticist.
Patient FAQ & Clinical Guidance
Q1: What is the HR gene and its role in Atrichia with Papular Lesions?
The HR gene encodes a protein that regulates hair follicle cycling, and biallelic loss‑of‑function mutations cause complete, irreversible hair loss with characteristic papules. (يُشفّر جين HR بروتينًا يُنظِّم دورة بصيلات الشعر، وتؤدي الطفرات المتنحية فيه إلى فقدان الشعر الدائم مع حطاطات جلدية مميزة.)
Q2: How is the sample collected and is a home visit available?
We offer a painless, hospital‑grade home blood draw or finger‑prick FTA card collection from 8 AM to 11 PM, ensuring cold‑chain integrity throughout the process. (نقدم خدمة سحب الدم المنزلي أو بطاقة FTA عبر وخز الإصبع من 8 صباحاً حتى 11 مساءً مع الحفاظ على سلسلة تبريد مثالية.)
Q3: Can this guide future treatments or fertility decisions?
A definitive genetic diagnosis informs recurrence risk for future pregnancies (25% if both parents are carriers) and may qualify for preimplantation genetic diagnosis or targeted research therapies. (يُحدد التشخيص الجيني القاطع خطر تكرار الإصابة في الأحمال المستقبلية (25%) وقد يرشد إلى التشخيص الجيني قبل الزرع أو العلاجات البحثية المستهدفة.)
دعم ثنائي اللغة متاح
التحقق من التغطية التأمينية
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