Test Price
2,800 AED✅ Home Collection Available
LPIN2 Gene Majeed Syndrome Genetic Test in UAE | 2800 AED | 2026 DHA Guidelines
تحليل الجين LPIN2 لمتلازمة ماجد بتقنية التسلسل الجيني من الجيل التالي في الإمارات | 2800 درهم | معتمد من هيئة الصحة بدبي
Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO‑accredited Next‑Generation Sequencing.
Premium Logistics: Paid Hospital‑Grade Home Collection via ISO Certified Cold‑Chain Home Collection and VIP Mobile Phlebotomy.
Clinical Guidance: Complimentary Telephonic Post‑Test Clinical Guidance for result interpretation.
Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731.
ضمان الدقة: حساسية تشخيصية 99.9% عبر تقنية تسلسل الجيل التالي المعتمدة من ISO.
الخدمات اللوجستية المتميزة: زيارة منزلية لجمع العينات بمواصفات المستشفيات عبر سلسلة تبريد معتمدة وخدمة سحب دم متنقلة VIP.
الإرشاد السريري: استشارة سريرية هاتفية مجانية بعد الفحص لتفسير النتائج.
التأمين: التحقق المباشر من تغطية التأمين عبر واتساب +971 54 548 8731.
Test Overview
This Next‑Generation Sequencing (NGS) test analyzes the entire LPIN2 gene to identify pathogenic mutations causing Majeed syndrome – a rare autoinflammatory disorder affecting bone (chronic recurrent multifocal osteomyelitis), skin (inflammatory dermatosis), and blood (congenital dyserythropoietic anemia). يكشف هذا التحليل الجيني الكامل عن الطفرات المسببة لمتلازمة ماجد، وهو اضطراب التهابي ذاتي نادر يشمل العظام والجلد والدم.
| Feature | Our Test (NGS) | Closest Alternative (Single‑Gene Sanger) |
|---|---|---|
| Precision | Full‑gene coverage, detects SNVs, indels, and CNVs with >99.9% analytical sensitivity | Limited to known point mutations; misses large deletions/duplications |
| Methodology | Next‑Generation Sequencing (Illumina platform) with bioinformatic validation | Sanger sequencing of individual exons |
| Turnaround Time | 3–4 weeks | 4–6 weeks (often with sequential testing) |
Clinical Context & Safety
“This molecular diagnosis provides definitive confirmation of Majeed syndrome; however, it must be interpreted alongside clinical evaluation, imaging studies, and laboratory markers. I strongly recommend pre‑ and post‑test genetic counselling to help families understand the autosomal recessive inheritance and reproductive options. Our multidisciplinary team is here to support you at every step.”
— Dr. Prabhakar Reddy, DHA License 61713011, Senior Clinical Geneticist
⚠ Medication Safety Notice
Do not discontinue prescribed medication without consulting your doctor.
Exclusion Criteria & Red Flags
- Exclusion Criteria: Insufficient or degraded DNA sample; collection on expired FTA card; active hemolysis interfering with extraction.
- Exclusion Criteria: Inability to provide informed consent (for minors, legal guardian consent mandatory under UAE CDS Law 2026).
- Red Flags for Urgent Care: Sudden severe bone pain, high fever (>39°C), pallor with dizziness, or any acute worsening of anemia – seek immediate medical attention.
Frequently Asked Questions
Q1: What is Majeed syndrome and how does this test help?
Snippet‑grade answer: Majeed syndrome is a rare autoinflammatory disorder caused by LPIN2 mutations, and this NGS test confirms the genetic diagnosis.
The LPIN2 gene mutation leads to chronic bone inflammation (osteomyelitis), anemic episodes, and skin rashes early in life. By sequencing the entire gene, we can identify the exact pathogenic variant, allowing precise diagnosis, carrier screening for family members, and informed management. متلازمة ماجد هي اضطراب التهابي ذاتي نادر ناتج عن طفرات في جين LPIN2، وهذا الفحص يؤكد التشخيص الوراثي بدقة.
Q2: What sample types are accepted for this test?
Snippet‑grade answer: We accept whole blood, extracted DNA, or a single drop of blood on an FTA card.
Home collection ensures a licensed phlebotomist draws a blood sample, which is then preserved on an FTA card or transported in EDTA tubes under cold‑chain protocol. Extracted DNA can also be submitted if guidelines are followed. نقبل عينة دم كامل، أو حمض نووي مستخلص، أو قطرة دم واحدة على بطاقة FTA.
Q3: How long do results take, and what support is provided?
Snippet‑grade answer: Turnaround time is 3‑4 weeks, and you will receive a telephonic clinical guidance session to explain the findings.
Our ISO‑certified laboratory processes the sample, and a board‑certified geneticist interprets the report. A complimentary post‑ consultation helps you understand the implications, including family planning and potential therapies. مدة النتائج 3−4 أسابيع، وستحصل على استشارة هاتفية مجانية بعد الفحص لشرح النتائج.
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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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