Test Price
2,800 AED✅ Home Collection Available
OBSL1 Gene (Three M Syndrome Type 2) Genetic Test in UAE | 2800 AED | 2026 DHA Guidelines
تحليل جين OBSL1 لمتلازمة ثري إم النوع الثاني في الإمارات | 2800 درهم | معتمد من هيئة الصحة بدبي
Executive Summary | ملخص تنفيذي
يُوفّر هذا التحليل الجيني المُعتمد من هيئة الصحة بدقة تشخيصية تصل إلى 99.9% مع استشارة وراثية سريرية متكاملة، وخدمة سحب منزلي عالية الجودة، وتوجيه طبي هاتفي بعد النتيجة.
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 accredited NGS processing.
- Premium Logistics: Hospital-Grade Home Collection (ISO Certified Cold-Chain) & VIP Mobile Phlebotomy.
- Clinical Guidance: Telephonic post-test clinical interpretation by a DHA-licensed specialist.
- Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731.
Overview
This next‑generation sequencing (NGS) test detects pathogenic variants in the OBSL1 gene, confirming a diagnosis of Three M syndrome type 2 (autosomal recessive primordial dwarfism). In the UAE, the analysis is performed under strict DHA regulatory oversight, combining clinical genetics expertise with state‑of‑the‑art molecular technology. يتيح التحليل تشخيصًا دقيقًا لمتلازمة ثري إم النوع الثاني بوساطة التسلسل الجيني فائق الإنتاجية وبإشراف طبي متخصص.
| Feature | Our Test (AMPLIHealth DHA‑lab) | Closest Alternative (Overseas lab) |
|---|---|---|
| Technology | NGS with full gene coverage & copy‑number analysis | Sanger sequencing of selected exons only |
| Reporting | Clinically curated, ACMG‑classified, 3‑4 weeks TAT | Technical raw data, up to 10 weeks |
| UAE Compliance | Full PDPL, CDS law, genetic counselling included | May not meet local data residency requirements |
Physician Insight & Safety Protocol
“As a clinical geneticist and DHA-licensed physician, I cannot overstate the importance of interpreting this test alongside a detailed dysmorphology evaluation and family history. The report is a powerful tool, but it does not replace the human touch of a skilled paediatrician. I always counsel families that a negative result does not exclude the condition if clinical suspicion remains high.” — Dr. PRABHAKAR REDDY, DHA License 61713011
⚠ Medication Warning: Do not discontinue prescribed medication or supplements without consulting your doctor. This genetic test does not provide guidance on medication management.
Exclusion Criteria & Emergency Red Flags
- Exclusion: Test not performed on minors without legal guardian consent (Federal Law No. 41/2024 & CDS 2026).
- Exclusion: Inadequate sample (degraded DNA, insufficient volume) requires recollection.
- ER Red Flag: If the patient develops acute respiratory distress, cyanosis, severe feeding intolerance, or signs of increased intracranial pressure, seek immediate emergency care – genetic testing is not a substitute for acute clinical management.
Patient FAQ & Clinical Guidance
What does the OBSL1 gene test detect and how is it used in UAE paediatric care?
This identifies disease‑causing mutations in the OBSL1 gene that confirm Three M syndrome type 2, a rare growth disorder characterised by prenatal and postnatal growth retardation, distinctive facial features, and skeletal anomalies. UAE paediatricians and neonatologists integrate the results with clinical and radiological findings to establish an accurate diagnosis, guide management, and offer genetic counselling for affected families. يكشف التحليل عن الطفرات المسببة للمرض في جين OBSL1 ويُستخدم مع التقييم السريري لتأكيد متلازمة ثري إم النوع الثاني عند الأطفال في الإمارات.
How long do results take and who will explain them?
Final reports are delivered within 3–4 weeks after sample receipt and are interpreted by a DHA‑licensed clinical geneticist or paediatrician during a dedicated telephonic consultation. The session covers variant classification, recurrence risk, and recommended follow‑up. تُسلَّم النتائج في غضون 3 إلى 4 أسابيع مع جلسة تفسير هاتفية من طبيب وراثة تابع لهيئة الصحة بدبي.
Is home sample collection available and how is privacy protected?
Yes, we offer paid hospital‑grade home collection (blood, extracted DNA, or FTA card) with ISO‑certified cold‑chain logistics across all emirates. All genetic data is handled strictly under the UAE PDPL and stored in DHA‑compliant secure servers with anonymised reporting. تتوفر خدمة سحب منزلي فائقة الجودة مع حماية كاملة للبيانات الجينية طبقًا لقانون حماية البيانات الشخصية الإماراتي.
ISO 9001:2015 Certified (Cert: INT/EGQ/2509DA/3139) | DHA Facility License: 9834453 | Support WhatsApp: +971 54 548 8731
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Stop the guesswork. Send a photo of your Insurance Card and Doctor's Prescription to our DHA-Certified Verification Team on WhatsApp.
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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