Test Price
2,800 AED✅ Home Collection Available
HPS3 Gene (Hermansky‑Pudlak Syndrome Type 3) Genetic Test in UAE | 2800 AED | 2026 DHA Guidelines
تحليل الجين HPS3 (متلازمة هيرمانسكي‑بودلاك النوع الثالث) بتقنية NGS في الإمارات | 2800 درهم | معتمد من هيئة الصحة بدبي
🔬 Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 Certified Processing. ضمان دقة تشخيصية بنسبة 99.9% عبر معالجة معتمدة من ISO 9001:2015.
🚚 Premium Logistics: Paid Hospital‑Grade Home Collection via ISO Certified Cold‑Chain Home Collection and VIP Mobile Phlebotomy. خدمة جمع العينات المنزلية بمعايير المستشفيات عبر فريق تمريض متنقل VIP وسلسلة تبريد معتمدة.
📞 Clinical Guidance: Telephonic Post‑Test Clinical Guidance in result interpretation. إرشاد سريري هاتفي بعد الفحص لتفسير النتائج.
💰 Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731. التحقق من التغطية التأمينية عبر واتساب على 971545488731+.
Pre‑Test Information
A detailed clinical history must be provided. A mandatory genetic counselling session is required to draw a pedigree of family members affected by the HPS3 gene mutation before sample collection.
Overview
The HPS3 Gene Genetic Test analyses the entire coding region of the HPS3 gene using Next‑Generation Sequencing to confirm or rule out Hermansky‑Pudlak syndrome type 3, an autosomal recessive disorder characterised by oculocutaneous albinism, platelet storage pool deficiency, and risk of pulmonary fibrosis. تحليل الجين HPS3 بتقنية NGS يؤكد أو يستبعد متلازمة هيرمانسكي‑بودلاك النوع الثالث، وهو اضطراب وراثي متنحٍ يتميز بالمهق العيني الجلدي ونقص حبيبات الصفائح وخطر التليف الرئوي.
| Feature | Our Test (Premium NGS) | Closest Alternative (Single‑Gene Sanger) |
|---|---|---|
| Precision | >99.9% analytical sensitivity; detects point mutations, small indels, copy‑number variants | High sensitivity for targeted regions, but limited scope |
| Method | Next‑Generation Sequencing (NGS) with full bioinformatics pipeline | Sanger sequencing – lower throughput, individual exon focus |
| Speed | 3 to 4 weeks (comprehensive analysis) | 2–4 weeks, but often requires multiple rounds |
| Sample | Blood, extracted DNA, or one drop blood on FTA card | Blood or extracted DNA |
Physician Insight & Safety Protocol
“As an ophthalmologist closely involved in Hermansky‑Pudlak syndrome care, I know that a genetic diagnosis brings clarity for vision‑sparing strategies, bleeding precautions, and lifelong pulmonary surveillance. This test should always be paired with expert clinical correlation – a positive result never stands alone, and a negative result in a strong clinical picture warrants further evaluation.” – Dr. PRABHAKAR REDDY (DHA: 61713011)
🚨 Medication Warning
Do not discontinue prescribed medication without consulting your doctor. Certain drugs (e.g., antiplatelets, anticoagulants) may be temporarily held only under written medical direction before blood draw.
Exclusion Criteria & Red Flags
- Individuals without clinical suspicion or a positive family history should seek genetic counselling first.
- Minors require documented parental consent as per UAE CDS Law 2026.
- Emergency red flags: sudden severe bleeding, acute vision loss, or unexplained bruising – proceed to the nearest ER immediately.
Patient FAQ & Clinical Guidance
What exactly does the HPS3 NGS test detect, and why is it important?
This sequences the entire HPS3 gene to identify disease‑causing mutations responsible for Hermansky‑Pudlak syndrome type 3, enabling definitive diagnosis, carrier detection, and tailored management of bleeding, vision, and lung risks. يكشف التحليل الطفرات المسببة للمرض في الجين HPS3 لتأكيد التشخيص وتحديد الحاملين ووضع خطة علاجية شخصية.
How is the sample collected, and is home service available in the UAE?
A certified phlebotomist collects a small blood sample (or accepts pre‑extracted DNA/FTA card) at your home, office, or our facility between 8 AM and 11 PM, with full cold‑chain integrity and VIP mobile service across all emirates. يتم سحب عينة الدم في المنزل أو العمل بواسطة فريق تمريض معتمد مع سلسلة تبريد كاملة وتغطية جميع الإمارات.
When will I receive my results, and can I discuss them with a specialist?
Results are delivered within 3–4 weeks through a secure portal, and a complimentary telephonic clinical guidance session with a genetic counsellor or ophthalmologist is included to explain the findings and next steps. تصدر النتائج خلال 3–4 أسابيع عبر بوابة آمنة، مع جلسة إرشاد هاتفية مجانية مع مستشار وراثي أو طبيب عيون لتفسير النتائج.
دعم ثنائي اللغة متاح
التحقق من التغطية التأمينية
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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.
Available in Arabic, English, Hindi & Urdu
ISMS 27001:2022
ISO Accredited
HIPAA
All reports reviewed by DHA-Certified physicians