Test Price
2,800 AED✅ Home Collection Available
MLPH Gene Griscelli Syndrome Type 3 Genetic Test in UAE | 2800 AED | 2026 DHA Guidelines
تحليل MLPH Gene Griscelli Syndrome Type 3 Genetic Test في الإمارات | 2800 درهم | معتمد من هيئة الصحة بدبي
Executive Summary: ملخص تنفيذي: تحليل جيني متقدم لمتلازمة جريسيللي من النوع 3 باستخدام تقنية التسلسل الجيني من الجيل التالي (NGS) بدقة تشخيصية تصل إلى 99.9% ومعتمد وفق معايير هيئة الصحة بدبي (DHA) لعام 2026، مع إمكانية السحب المنزلي والتأمين المباشر.
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 (Cert: INT/EGQ/2509DA/3139) Accredited Processing.
- Premium Logistics: Paid Hospital-Grade Home Collection via ISO Certified Cold-Chain Home Collection and VIP Mobile Phlebotomy (8 AM – 11 PM).
- Clinical Guidance: Telephonic Post-Test Clinical Guidance in result interpretation by DHA-licensed specialists.
- Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731.
Overview
This advanced Genetic Test specifically screens the MLPH gene to confirm or rule out Griscelli syndrome type 3, a rare autosomal recessive hypopigmentation disorder presenting with silvery-gray hair and skin depigmentation. هذا الفحص الجيني المتقدم يفحص جين MLPH لتأكيد أو استبعاد متلازمة جريسيللي من النوع 3، وهو اضطراب وراثي نادر يتميز بشعر فضي وبقع جلدية فاتحة.
| Feature | Our Test (MLPH NGS) | Closest Alternative (Sanger Sequencing) |
|---|---|---|
| Precision | Full gene coverage (all exons, splice sites) | Targeted mutation analysis only |
| Methodology | Next-Generation Sequencing (NGS) | Sanger Sequencing (single amplicons) |
| Turnaround | 3–4 Weeks | 6–8 Weeks (by referral labs) |
| Home Collection | Available (Cold-Chain) | Often Not Available |
Physician Insight & Safety Protocol
“As a dermatologist, I emphasize that Griscelli syndrome type 3 manifests exclusively with cutaneous hypopigmentation, without the immune or neurological complications seen in types 1 and 2. Genetic confirmation via this test guides precise counseling and differentiates it from Chediak–Higashi syndrome. Always correlate molecular findings with clinical phenotype and family history.”
— Dr. PRABHAKAR REDDY, DHA License No.: 61713011, Senior Consultant Dermatologist and Genetic Medicine
⚠️ Medication Warning: Do not discontinue prescribed medication without consulting your doctor.
Safety Exclusion Criteria & ER Red Flags
- Exclusion Criteria: Patients with active systemic infection, coagulopathy contraindicating venipuncture, or inability to provide informed consent.
- Emergency Red Flags: If the patient exhibits fever, hepatosplenomegaly, or neurological deterioration (suggestive of hemophagocytic lymphohistiocytosis or Griscelli types 1/2), immediate emergency medical evaluation is mandatory—this genetic test is not a substitute for acute care.
- Pediatric/Minor Consent: In compliance with UAE CDS Law 2026 (Minors), all testing of individuals under 18 requires legal guardian consent and certified genetic counseling.
Legal & Accreditation Compliance
- This diagnostic service adheres to Federal Decree-Law No. 41 of 2024, Article 87, governing genetic data privacy and biobank management.
- Child Data Sharing (CDS) Law 2026 strictly enforced for minors; all results are encrypted and shared only with authorized guardians.
- Full compliance with UAE PDPL (Federal Decree-Law No. 45 of 2021) for personal data protection; your genetic information is stored securely in Dubai Health Authority (DHA) licensed facilities.
- ISO 9001:2015 Certified (Certificate: INT/EGQ/2509DA/3139), DHA/MOHAP Facility License No. 9834453.
Patient FAQ & Clinical Guidance
1. What is the MLPH gene test for Griscelli syndrome type 3?
This Genetic Test detects MLPH gene mutations causing Griscelli syndrome type 3, a hypopigmentation disorder, with high accuracy.
هذا الفحص الجيني بتقنية التسلسل الجيني (NGS) يكشف الطفرات في جين MLPH المسببة لمتلازمة جريسيللي من النوع 3، وهي اضطراب في تصبغ الجلد والشعر، بدقة عالية.
2. How is the performed and what sample is required?
A blood sample or DNA on FTA card is collected at home and analyzed via NGS for MLPH gene mutations.
يتم جمع عينة دم أو حمض نووي على بطاقة FTA منزليًا عن طريق ممرض معتمد، ثم تُحلل بتقنية NGS لاكتشاف طفرات جين MLPH.
3. How long do results take and what is the cost?
Results are ready in 3 to 4 weeks, priced at 2800 AED with direct insurance billing via WhatsApp support.
تصدر النتائج خلال 3 إلى 4 أسابيع، بتكلفة 2800 درهم إماراتي مع إمكانية الفوترة المباشرة للتأمين عبر واتساب.
Book Your Home Collection or Get a Quote
WhatsApp: +971 54 548 8731
DHA License No. 9834453 • ISO 9001:2015
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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