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2,800 AED

✅ Home Collection Available

MTTP Gene Sequencing for Abetalipoproteinemia in UAE | 2800 AED | 2026 DHA Guidelines

تحليل تسلسل جين MTTP للكشف عن انعدام البروتين الشحمي بيتا في الإمارات | 2800 درهم | معتمد من هيئة الصحة بدبي

الخلاصة التنفيذية

فحص جيني فائق الدقة (حساسية تشخيصية 99.9%) لتسلسل جين MTTP باستخدام تقنية التسلسل الجيلي القادم (NGS) عبر مختبر معتمد آيزو 9001:2015. السحب المنزلي للمستشفى المدفوع مسبقاً مع نقل مبرد معتمد، يليه توجيه سريري هاتفي بعد النتيجة. التحقق من التغطية التأمينية متاح عبر واتساب +971 54 548 8731.

Executive Summary

  • Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 Certified NGS Processing.
  • Premium Logistics: Paid Hospital-Grade Home Collection via ISO Certified Cold-Chain Phlebotomy & VIP Mobile Service (8 AM – 11 PM).
  • Clinical Guidance: Complimentary Telephonic Post‑Test Interpretation by a DHA‑licensed specialist.
  • Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731.

Overview

The MTTP Gene Full Sequencing test detects pathogenic variants in the microsomal triglyceride transfer protein gene causing abetalipoproteinemia, a rare autosomal recessive disorder of lipid metabolism. This definitive DNA analysis replaces older phenotypic screening with a 3‑week NGS workflow, delivering the most precise molecular confirmation available in the UAE.

Feature Our Test (MTTP NGS) Closest Alternative
Precision Full gene sequencing with CNV detection Limited hotspot panel or biochemical assays only
Methodology NGS (Next Generation Sequencing) + Sanger validation Sanger sequencing of selected exons
Turnaround 3–4 Weeks (from sample receipt) 6–8 Weeks (multi-step send‑out)

Physician Insight & Safety Protocol

“A positive MTTP result must be correlated with clinical findings, lipoprotein electrophoresis, and fat‑soluble vitamin levels. A negative report, while reassuring, does not eliminate the need for ongoing monitoring in symptomatic patients. Never make therapeutic decisions solely on this gene test without a comprehensive metabolic evaluation.”
– Dr. PRABHAKAR REDDY, DHA License: 61713011

⚠ Medication Warning: Do not discontinue prescribed medication or lipid‑lowering therapy without consulting your treating physician. This genetic test is diagnostic, not prescriptive.

Exclusion Criteria & Emergency Red Flags

  • Active severe infection or acute metabolic decompensation – postpone sample collection.
  • Inability to provide informed consent (mandatory pre‑test genetic counselling).
  • If patient exhibits severe steatorrhea, failure to thrive in infancy, or progressive ataxia, seek immediate specialist care alongside testing.

Patient FAQs & Clinical Guidance

1. How long does it take to get my MTTP gene test results in the UAE?

Your NGS‑based MTTP gene sequencing report is typically ready within 3 to 4 weeks from the moment our laboratory receives your blood, DNA FTA card, or extracted DNA sample. This timeline includes full bioinformatics analysis and expert clinical interpretation for abetalipoproteinemia.

2. هل أحتاج إلى وصفة طبية لإجراء فحص جين MTTP في الإمارات؟

لا يُطلب وصفة طبية إلزامية، ولكننا نوصي بشدة بجلسة استشارة وراثية قبل الفحص لرسم شجرة العائلة وتوثيق التاريخ المرضي لعائلة مصابة بانعدام البروتين الشحمي بيتا. هذا يضمن التفسير الدقيق للنتيجة.

(No prescription is mandatory, but we strongly recommend a pre‑test genetic counselling session to draw a pedigree chart and document the clinical history of family members with abetalipoproteinemia. This ensures accurate result interpretation.)

3. Can this test be performed on an infant or child in compliance with UAE law?

Yes, paediatric testing is permissible under UAE Federal Decree‑Law No. 41 of 2024 and the 2026 CDS Law, provided valid guardian consent is obtained and a paediatric metabolic specialist oversees the post‑ follow‑up. Our home collection team is trained in neonatal and paediatric phlebotomy.

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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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