Test Price
2,800 AED✅ Home Collection Available
ABCA1 Gene HDL Deficiency Type 2 Genetic Test in UAE | AED 2800 | 2026 DHA Guidelines
تحليل جين ABCA1 لنقص الكولستيرول الجيد HDL من النوع الثاني في الإمارات | 2800 درهم | معتمد من هيئة الصحة بدبي
Executive Summary
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 Accredited Processing.
- Premium Logistics: Hospital-Grade Home Collection with ISO Certified Cold-Chain, VIP Mobile Phlebotomy available 8 AM – 11 PM.
- Clinical Guidance: Complimentary post-test telephonic consultation for result interpretation.
- Insurance: Direct billing verification via WhatsApp at +971 54 548 8731.
ملخص تنفيذي: نضمن دقة تشخيصية بنسبة 99.9% عبر مختبر معتمد ISO 9001:2015، مع خدمة سحب منزلي متميزة واستشارة طبية مجانية بعد النتيجة. نلتزم بقوانين دولة الإمارات وخصوصية البيانات.
Clinical Overview
The ABCA1 Gene NGS Test sequences the entire ABCA1 coding region to diagnose familial HDL deficiency type 2, characterized by extremely low HDL cholesterol and heightened cardiovascular risk. يتم إجراء التحليل بتقنية تسلسل الجيل التالي لتحديد الطفرات الوراثية بدقة متناهية.
| Feature | Our Test (NGS) | Standard Lipid Panel | Targeted Genotyping |
|---|---|---|---|
| Precision | >99.9% analytical sensitivity/specificity | Does not detect genetic cause | Limited to known hotspots |
| Methodology | Next-Generation Sequencing (full gene) | Enzymatic colorimetric | PCR-based SNP arrays |
| Turnaround | 3–4 Weeks | 24 Hours | 1–2 Weeks |
| Clinical Utility | Definitive diagnosis, family screening | Phenotypic lipid assessment only | May miss novel mutations |
Physician Insight & Safety Protocol
“Genetic testing for lipid disorders demands careful clinical correlation. A positive ABCA1 result must be interpreted alongside your full lipid profile and family history; a negative result does not exclude other causes of severely low HDL. Please maintain all specialist appointments and never discontinue prescribed statins or other medications without my direct instruction.”
— Dr. Prabhakar Reddy, DHA License: 61713011
Safety Notice: Do not discontinue prescribed medication without consulting your doctor.
Exclusion Criteria for Blood Draw:
- Active febrile illness or systemic infection
- Recent blood transfusion (<3 months)
- Known coagulopathy (inform phlebotomist)
- Pregnancy (notify the collection specialist)
Emergency Red Flags (Seek Immediate Care):
- Sudden chest pain, pressure, or dyspnea
- Signs of stroke: facial droop, unilateral weakness, speech difficulty
- Severe dizziness or loss of consciousness
This test does not replace urgent cardiovascular evaluation. If symptoms arise, proceed to the nearest emergency department.
Frequently Asked Questions & Clinical Guidance
1. What is the ABCA1 Gene HDL Deficiency Type 2 NGS Test?
Snippet: This NGS test identifies ABCA1 gene mutations causing familial HDL deficiency type 2 for accurate diagnosis and personalized cardiovascular risk assessment.
The test uses next-generation sequencing to analyze the entire ABCA1 gene, detecting pathogenic variants linked to Tangier disease and severe hypoalphalipoproteinemia. It is essential for confirming a genetic diagnosis when HDL cholesterol is persistently below 20 mg/dL, and for guiding family cascade screening.
س: ما هو تحليل جين ABCA1 لنقص HDL من النوع الثاني؟
ج: يكشف تحليل تسلسل الجيل التالي عن طفرات جين ABCA1 المسؤولة عن نقص الكوليسترول الجيد الحاد، مما يتيح تشخيصًا دقيقًا وتقييمًا شاملاً لمخاطر القلب والأوعية الدموية.
2. Who should consider this genetic test in the UAE?
Snippet: Individuals with persistent extremely low HDL cholesterol, premature coronary artery disease, or a family history of Tangier disease should consider this test.
The test is recommended for patients presenting with HDL levels < 20 mg/dL, enlarged orange tonsils, hepatosplenomegaly, or unexplained neuropathy. Additionally, first-degree relatives of a confirmed carrier benefit from predictive testing under the UAE CDS Law 2026 minor consent protocols.
س: من يجب أن يخضع لهذا التحليل في الإمارات؟
ج: يُوصى به للأشخاص الذين يعانون من انخفاض حاد ومستمر في الكوليسترول الجيد أو لديهم تاريخ عائلي لداء تنغيير، ويُجرى وفق أحدث توجيهات هيئة الصحة بدبي.
3. How is the performed and how long do results take?
Snippet: A simple blood sample is collected via home VIP phlebotomy, then analyzed via NGS with results typically available within 3 to 4 weeks.
After booking, a certified phlebotomist arrives at your location between 8 AM and 11 PM. The sample is transported in a temperature-controlled cold chain to our ISO-certified laboratory. Once sequencing is complete, a comprehensive report is delivered, and a specialist teleconsultation is scheduled to explain findings.
س: كيف يتم إجراء التحليل وكم يستغرق؟
ج: يُسحب عينة دم بسيطة بواسطة فريق تمريض منزلي متمرس، وتُحلل بتقنية NGS، وتصدر النتائج خلال 3 إلى 4 أسابيع مع استشارة طبية مجانية.
UAE Regulatory & Quality Compliance
This service adheres to Federal Decree-Law No. 41 of 2024 (Article 87), UAE CDS Law 2026 concerning minors, and the UAE Personal Data Protection Law (PDPL). Our laboratory holds ISO 9001:2015 certification INT/EGQ/2509DA/3139 and DHA Facility License No. 9834453. All genetic data is processed exclusively within the United Arab Emirates.
WhatsApp Support & Booking: +971 54 548 8731
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All reports reviewed by DHA-Certified physicians