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Test Price

2,800 AED

✅ Home Collection Available

DLD Gene Maple Syrup Urine Disease Type 3 Genetic Test in UAE | 2800 AED | 2026 DHA Guidelines

تحليل جين DLD لمرض بول شراب القيقب من النوع الثالث بتقنية التسلسل الجيني الشامل (NGS) في الإمارات | 2800 درهم إماراتي | معتمد من هيئة الصحة بدبي

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.

تحليل جيني دقيق ومعتمد وفقًا لأعلى معايير هيئة الصحة بدبي لضمان سلامة المرضى في دولة الإمارات.

Test Overview

The DLD Gene NGS test detects mutations causing Maple Syrup Urine Disease Type 3, a severe metabolic disorder. This test utilizes Next Generation Sequencing for comprehensive gene analysis, offering rapid and precise diagnostic clarity for patients in the UAE.

Feature Our Test Closest Alternative
Precision (Analytical Sensitivity) 99.9% ~96% (limited panel)
Methodology Next Generation Sequencing (NGS) – Full Gene Sanger sequencing / targeted mutation panel
Turnaround Time 3–4 Weeks 4–6 Weeks

Physician Insight & Safety Protocol

“As a DHA-licensed physician, I encourage patients to view this test as one piece of the diagnostic puzzle. A positive result requires clinical correlation, and a negative result does not entirely exclude the disease. Please discuss all results with your doctor before making any health decisions.”

— Dr. PRABHAKAR REDDY, DHA License: 61713011

⚠️ Medication Warning:

Do not discontinue prescribed medication without consulting your doctor.

Exclusion Criteria & Emergency Red Flags

  • Exclusion: This test is not for acute crisis management; patients with severe neurological symptoms should seek emergency care immediately. Not suitable for individuals with recent blood transfusion (within 4 weeks) if DNA is extracted from whole blood.
  • ER Red Flag: Seek emergency medical attention if the patient experiences lethargy, vomiting, seizures, or coma – these may indicate a metabolic crisis.

Pre‑Test Information

A Genetic Counselling session to draw a pedigree chart of family members affected with Maple Syrup Urine Disease Type 3 is mandatory before sample collection. Clinical history including metabolic symptoms, dietary management, and prior newborn screening results must be provided.

Patient FAQ & Clinical Guidance

Q: What is the DLD Gene Maple Syrup Urine Disease Type 3 NGS Test?

This test sequences the entire DLD gene to detect mutations responsible for Maple Syrup Urine Disease Type 3, a rare inherited metabolic disorder that impairs the breakdown of branched‑chain amino acids. (تحليل الجين DLD للكشف عن مرض بول شراب القيقب من النوع الثالث.)

Q: Why is genetic counseling recommended before this test?

Pre‑test genetic counseling ensures you understand the implications of carrier status for family planning, future pregnancies, and clinical management, aligning with UAE family‑centred care. (يوصى بجلسة استشارة وراثية قبل الاختبار لتقييم التاريخ العائلي والمخاطر المحتملة.)

Q: How accurate is this NGS and what is the turnaround time?

With >99.9% analytical sensitivity validated by ISO 9001:2015 accredited laboratories, this Next Generation Sequencing panel provides a definitive diagnosis for Maple Syrup Urine Disease Type 3; results are available within 3 to 4 weeks from sample receipt. (بنسبة دقة تزيد عن 99.9%، تظهر النتائج خلال 3 إلى 4 أسابيع.)

Regulatory Compliance: Federal Decree‑Law No. 41 of 2024 (Art. 87), CDS Law 2026 (Minors), UAE PDPL (Data Privacy), DHA/MOHAP Standards.

ISO 9001:2015 Certified: Cert: INT/EGQ/2509DA/3139 | Facility License: 9834453

Support & WhatsApp: +971 54 548 8731 (8 AM – 11 PM, daily)

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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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