Test Price
2,800 AED✅ Home Collection Available
CSF1 Gene Osteogenesis and Dental Anomalies Genetic Test in UAE | 2800 AED | 2026 DHA Guidelines
تحليل جين CSF1 لتخلق العظام والتشوهات السنية في الإمارات | 2800 درهم | معتمد من هيئة الصحة بدبي
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 certified NGS processing.
- Premium Logistics: Hospital‑grade home collection (cold‑chain transport) & VIP mobile phlebotomy – 8 AM‑11 PM daily.
- Clinical Guidance: Complimentary telephonic post‑test genetic counselling for result interpretation.
- Insurance: Direct billing verification via WhatsApp +971 54 548 8731.
الملخص التنفيذي
يضمن هذا الفحص الجيني المتقدم تحليل تسلسل الجينوم الكامل لجين CSF1 بدقة تشخيصية تبلغ 99.9% عبر مختبر معتمد بموجب ISO 9001:2015. تشمل الخدمة سحب الدم المنزلي المبرد بتقنية سلسلة نقل مبردة، واستشارة وراثية هاتفية بعد الحصول على النتيجة لضمان فهمها السريري. للتحقق من التغطية التأمينية، يرجى التواصل عبر واتساب على الرقم: +971 54 548 8731.
About the Test
This next‑generation sequencing (NGS) assay thoroughly evaluates the entire coding region and exon‑intron boundaries of the CSF1 gene, delivering a molecular diagnosis for autosomal recessive osteopetrosis, dental anomalies, and associated pigmentation disorders. With a 3‑to‑4‑week turnaround, the test attains 99.9% sensitivity and specificity, performed in a DHA‑licensed facility (License 9834453) under strict ISO 9001:2015 quality standards.
| Feature | Our NGS Test | Closest Alternative (Sanger) |
|---|---|---|
| Test Coverage | Full gene & flanking regions | Selected exons only |
| Analytical Sensitivity | 99.9% | ~95% |
| Turnaround Time | 3 – 4 weeks | 6 – 8 weeks |
| Copy Number Variant Detection | Yes | Limited |
| Home Collection (cold chain) | Included | Not available |
Clinical Insight & Safety Protocol
“A confirmed genetic diagnosis provides families with clarity and a pathway to targeted management—never lose hope.” Dr. PRABHAKAR REDDY (DHA: 61713011) adds: “This NGS test is a powerful tool, but results must be correlated with the clinical picture. I strongly urge pre‑ and post‑test genetic counselling to avoid misinterpretation and to ensure all safety precautions are respected.”
Exclusion Criteria & Emergency Red Flags
- Patients under 12 years require a legal guardian’s written consent.
- Active systemic infection or recent blood transfusion (within 2 weeks) may affect sample quality.
- Pregnancy is not a contraindication, but post‑test counselling should cover prenatal implications.
- Seek urgent medical attention if you experience excessive bleeding, expanding haematoma, high fever, or signs of allergic reaction after the blood draw.
أسئلة شائعة / Frequently Asked Questions
Q: What conditions does the CSF1 gene test detect?
Snippet: This test detects mutations in the CSF1 gene linked to autosomal recessive osteopetrosis, dental anomalies, and pigmentation abnormalities. It screens for pathogenic variants that cause bone sclerosis, delayed tooth eruption, and skin hyperpigmentation, helping clinicians confirm a molecular diagnosis and guide specialist referrals.
س: ما الحالات التي يكشفها تحليل جين CSF1؟
يكشف هذا الفحص الطفرات في جين CSF1 المرتبطة بتصلب العظام الوراثي المتنحي، تشوهات الأسنان، واضطرابات التصبغ الجلدي. يساعد في تأكيد التشخيص الجزيئي وتوجيه الرعاية الطبية المتخصصة.
Q: How is the sample collected for this?
Snippet: A simple blood draw or a single drop of blood on an FTA card is all that is required. Our DHA‑licensed phlebotomists perform a painless venepuncture using cold‑chain transport to preserve DNA integrity, or you can provide extracted DNA if already available.
س: كيف يتم جمع العينة لهذا الفحص؟
يتم سحب عينة دم بسيطة أو وضع قطرة دم واحدة على بطاقة FTA، بواسطة أخصائي سحب دم مرخص من هيئة الصحة بدبي مع نقل مبرد للحفاظ على الحمض النووي.
Q: How long until I receive the results, and what support is provided?
Snippet: Results are typically available in 3 to 4 weeks, including a telephonic genetic counselling session to interpret the findings. You will receive a comprehensive report with variant classification and recommendations for clinical follow‑up, all coordinated through our ISO‑certified workflow.
س: متى تظهر النتائج وما الدعم المتوفر بعدها؟
تتوفر النتائج عادةً خلال 3 إلى 4 أسابيع، وتشمل جلسة إرشاد وراثي هاتفية لتفسير التقرير الجيني وتقديم التوصيات الطبية المناسبة.
UAE Regulatory Compliance & Data Privacy
- Federal Decree‑Law No. 41 of 2024 (Art. 87) – Genetic testing is performed with strict adherence to clinical necessity and licensed practice regulations.
- CDS Law 2026 (Minors) – Testing of individuals under 18 is conducted only with full guardian consent and paediatric genetic counselling.
- UAE PDPL (Federal Law No. 45 of 2021) – All personal data and genetic information are stored in encrypted, HIPAA‑aligned servers, accessible only to authorised clinical staff.
- ISO 9001:2015 Certified – Certificate No. INT/EGQ/2509DA/3139, DHA Facility License 9834453.
دعم ثنائي اللغة متاح
التحقق من التغطية التأمينية
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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.
Available in Arabic, English, Hindi & Urdu
ISMS 27001:2022
ISO Accredited
HIPAA
All reports reviewed by DHA-Certified physicians