Test Price
2,800 AED✅ Home Collection Available
AK2 Gene Reticular Dysgenesis Genetic Test in UAE | 2800 AED | 2026 DHA Guidelines
تحليل جين AK2 لخلل التنسج الشبكي بتقنية التسلسل الجيني من الجيل التالي في الإمارات | 2800 درهم | معتمد من هيئة الصحة بدبي 2026
Executive Summary | ملخص تنفيذي
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 Accredited Processing (Cert: INT/EGQ/2509DA/3139).
- 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 genetic counsellors.
- Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731.
نضمن حساسية تشخيصية بنسبة 99.9% عبر معالجة معتمدة وفقًا لمعيار آيزو، مع خدمة سحب منزلي متميزة وإرشاد طبي بعد الفحص.
Test Overview
The AK2 Gene Reticular Dysgenesis Genetic Test analyses the entire coding region of the AK2 gene to detect pathogenic variants causing this severe form of combined immunodeficiency (SCID). This next‑generation sequencing assay provides a definitive molecular diagnosis for affected individuals, family members, and suspected carriers, delivering a structured clinical report aligned with 2026 international guidelines. يُعتبر هذا التحليل الجيني الشامل الأداة التشخيصية الأكثر دقة لتأكيد الإصابة بخلل التنسج الشبكي الناجم عن طفرات جين AK2.
| Feature | Our Test (AK2 NGS) | Closest Alternative (Sanger Sequencing) |
|---|---|---|
| Precision | 99.9% analytical sensitivity & specificity; covers full coding region ± 20 bp intronic boundaries | 99.9% for targeted region only; limited to known hotspots |
| Method | Next‑Generation Sequencing (NGS) – Illumina platform, read depth > 100× | Sanger Sequencing – lower throughput, single amplicon approach |
| Turnaround | 3–4 Weeks (expedited available) | 6–8 Weeks for full gene (multiple fragments) |
Physician Insight & Safety Protocol
As Dr. PRABHAKAR REDDY (DHA: 61713011), Medical Director, I emphasise that this test must be correlated with the patient’s clinical presentation, immunological workup, and family history; a negative result does not exclude other forms of SCID or atypical presentations. The diagnosis of reticular dysgenesis carries profound implications for treatment, including urgent hematopoietic stem cell transplantation, and should only be interpreted by a multidisciplinary team. I strongly recommend genetic counselling prior to sample collection to ensure informed consent and psychosocial preparedness.
⛔ Medication Warning
Do not discontinue prescribed medication without consulting your doctor. Immunosuppressive therapy, immunoglobulin replacement, or antimicrobial prophylaxis must be maintained as directed by your treating physician. Abrupt cessation could trigger life‑threatening infections.
⚠️ Exclusion Criteria & ER Red Flags
- Acute febrile illness or uncontrolled infection at time of blood draw – reschedule.
- Recently transfused (< 2 weeks) – may cause sample contamination; notify lab.
- Emergency signs requiring immediate hospital visit: severe respiratory distress, high fever unresponsive to antipyretics, or signs of septic shock.
- Minors must have legal guardian consent per CDS Law 2026 provisions.
Patient FAQ & Clinical Guidance
1. What is the clinical utility of the AK2 gene test for reticular dysgenesis?
The AK2 Genetic Test definitively confirms reticular dysgenesis by detecting biallelic pathogenic variants, enabling targeted treatment planning and family cascade screening. يؤكد التحليل الجيني لجين AK2 وجود طفرات ممرضة في الجين، مما يسمح بوضع خطة علاجية دقيقة وفحص الأقارب.
2. How is the sample collected and what are the pre‑test requirements?
A mandatory genetic counselling session to construct a pedigree chart is required before collecting blood or DNA FTA card sample under cold‑chain conditions. يجب عقد جلسة استشارة وراثية لإنشاء شجرة العائلة قبل أخذ العينة بطريقة معتمدة.
3. Is this covered by UAE insurance and what data privacy laws apply?
We verify direct billing with major UAE insurers via WhatsApp at +971545488731; your genomic data is protected under Federal Decree‑Law No. 41 of 2024 and UAE PDPL. نحن نتحقق من التغطية التأمينية مباشرة، وتُحمى بياناتك الجينية بموجب المرسوم بقانون اتحادي رقم 41 لسنة 2024 وقانون حماية البيانات الشخصية الإماراتي.
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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.
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All reports reviewed by DHA-Certified physicians