Test Price
2,800 AED✅ Home Collection Available
IKBKG Gene Incontinentia Pigmenti Type 2 Genetic Test in UAE | 2800 AED | 2026 DHA Guidelines
تحليل جين IKBKG لمرض السلس الصباغي النوع 2 في الإمارات | 2800 درهم | معتمد من هيئة الصحة بدبي
Executive Summary
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO Accredited Processing.
- Premium Logistics: Paid Hospital-Grade Home Collection via ISO Certified Cold-Chain Home Collection and VIP Mobile Phlebotomy.
- Clinical Guidance: Telephonic Post-Test Clinical Guidance in result interpretation.
- Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731.
هذا الفحص الجيني المتطور لمرض السلس الصباغي من النوع الثاني معتمد وفق أعلى معايير هيئة الصحة بدبي لعام 2026، ويوفر أعلى دقة تشخيصية مع خدمة سحب منزلي آمنة وفورية ومطابقة للمواصفة ISO 9001:2015.
Clinical Overview & Diagnostic Superiority
The IKBKG NGS test detects pathogenic variants causing Incontinentia Pigmenti type 2, a rare X‑linked dominant disorder with skin, dental, ocular, and CNS features. This comprehensive sequencing covers all exons and splice junctions, enabling definitive molecular diagnosis and personalized management.
يُعتبر فحص جين IKBKG الأساسي لتأكيد تشخيص السلس الصباغي، حيث يغطي جميع الطفرات الجينية بدقة متناهية وفق أحدث تقنيات التسلسل من الجيل التالي.
| Parameter | Our Test – IKBKG NGS (Premium) | Closest Alternative – Single-Gene Sanger Sequencing |
|---|---|---|
| Precision / Method | Next Generation Sequencing – full gene coverage, detects point mutations, small indels, and copy number variants | Targeted Sanger sequencing – limited to preselected exons, may miss large deletions/duplications |
| Diagnostic Sensitivity | >99.9% for known pathogenic IKBKG variants | ~85–90% (deletion/duplication not assessed) |
| Turnaround Time | 3–4 Weeks (including clinical interpretation) | 6–8 Weeks |
| Clinical Report | DHA‑standard, with genetic counselling support and actionable recommendations | Basic variant listing without full integrative guidance |
Physician Insight & Safety Protocol
“As a clinician, I understand that pursuing a genetic diagnosis can be emotionally challenging. This IKBKG test provides families with definitive answers, but results must always be interpreted in the full clinical context. Early identification allows coordinated care for skin, dental, and neurological manifestations.”
— Dr. PRABHAKAR REDDY, DHA License 61713011
Medication Warning
Clinical notice: Do not discontinue any prescribed medication or alter treatment based on genetic test results without explicit consultation with your treating physician.
Exclusion Criteria & Emergency Red Flags
- Exclusion: Active systemic infection, severe bleeding diathesis, or inability to provide informed consent (legal guardian required for minors).
- Exclusion: Home collection must be deferred if you have a fever >38°C or acute dermatitis at the venipuncture site.
- ER Red Flag: Intense pain, uncontrolled bleeding, or signs of infection (redness, warmth, pus) at the collection site – seek immediate medical attention.
- ER Red Flag: Neurological symptoms such as sudden severe headache, visual loss, or seizures during the testing period require emergency evaluation unrelated to the test.
Frequently Asked Questions (Bilingual Clinical Guidance)
Q: What does the IKBKG genetic test diagnose?
A: It identifies IKBKG mutations causing Incontinentia Pigmenti, a rare X-linked condition impacting skin, eyes, and brain. The test is definitive for type 2 disease, confirming the molecular basis and guiding multisystem surveillance.
يكتشف هذا الفحص الطفرات في جين IKBKG المسببة لمرض السلس الصباغي النوع 2، وهو اضطراب نادر مرتبط بالصبغي X يؤثر على الجلد والعين والجهاز العصبي.
Q: How is the test performed and what sample is required?
A: A home blood sample is sequenced by NGS to detect IKBKG mutations causing Incontinentia Pigmenti. We accept whole blood, extracted DNA, or a single blood drop on an FTA card collected during VIP home phlebotomy.
يتم جمع عينة دم منزلياً عبر خدمة السحب المنزلي المعتمدة، ثم تُحلل بتقنية التسلسل من الجيل التالي. يُقبل الدم الكامل أو الحمض النووي المستخلص أو بطاقة FTA.
Q: What is the turnaround time and cost?
A: Fast turnaround of 3–4 weeks at 2800 AED, with expert genetic counseling and DHA-approved reporting. The price includes pre-test counselling, sample logistics, and post- clinical guidance.
تصدر النتائج خلال 3–4 أسابيع بتكلفة 2800 درهم، وتشمل استشارة وراثية معتمدة وتقريراً طبياً متوافقاً مع هيئة الصحة بدبي.
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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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ISMS 27001:2022
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