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2,800 AED

✅ Home Collection Available

TRAPPC11 Gene Limb‑Girdle Muscular Dystrophy, Autosomal Recessive Type 2S (LGMD‑2S) Genetic Test in UAE | 2800 AED | 2026 DHA Guidelines

تحليل جين TRAPPC11 للحثل العضلي الطرفي من النمط الجسدي المتنحي 2S (LGMD‑2S) في الإمارات | 2800 درهم | معتمد من هيئة الصحة بدبي

الملخص التنفيذي: يوفر هذا الفحص الجيني دقة تشخيصية 99.9% عبر مختبرنا المعتمد آيزو 9001:2015، مع خدمة سحب منزلي متميزة وسلسلة تبريد ذكية واستشارة هاتفية بعد النتيجة.

  • Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 Accredited Processing (Cert: INT/EGQ/2509DA/3139).
  • Premium Logistics: Hospital‑Grade Home Collection via ISO‑Certified Cold‑Chain Home Collection & VIP Mobile Phlebotomy (8 AM – 11 PM).
  • Clinical Guidance: Telephonic Post‑Test Clinical Guidance with result interpretation by a DHA‑licensed genetic specialist.
  • Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731.

Clinical Overview

The TRAPPC11 Gene NGS Test identifies pathogenic variants linked to autosomal recessive limb‑girdle muscular dystrophy type 2S (LGMD‑2S), enabling precise diagnosis, prognosis, and family risk stratification. يحدد اختبار جين TRAPPC11 الطفرات المسببة للضعف العضلي الطرفي من النمط 2S لتشخيص دقيق وتقييم المخاطر العائلية.

Feature Our TRAPPC11 NGS Test (ISO‑Lab) Closest Alternative (Standard Genetic Screening)
Methodology Next‑Generation Sequencing (NGS) – full gene coverage Sanger sequencing of selected exons or targeted panel
Diagnostic Precision 99.9% analytical sensitivity & >99% specificity Variable; may miss deep intronic or copy‑number variants
Turnaround Time 3–4 Weeks 4–8 Weeks
Sample Type Whole Blood, DNA FTA Card, or Extracted DNA Whole Blood only

Physician Insight & Safety Protocol

Dr. Prabhakar Reddy (DHA: 61713011): “This test provides critical insight into a rare muscle disease, but a genetic finding must always be correlated with the clinical picture, electromyography, and muscle biopsy results. I encourage families to pair the result with genetic counselling to fully understand inheritance and future planning. A negative report does not exclude other limb‑girdle dystrophies.”

Do not discontinue any prescribed medication or alter your rehabilitation plan without consulting your treating neurologist.

Exclusion Criteria & Emergency Red Flags

  • Acute febrile illness or systemic infection within 48 hours before sample collection.
  • Known haematological malignancy requiring urgent specialist clearance.
  • Severe cutaneous condition at venipuncture site or extreme needle phobia (contact lab for alternative collection).
  • ER Red Flags: Sudden worsening muscle weakness, difficulty breathing or swallowing, dark cola‑coloured urine (rhabdomyolysis), or unexplained falls – seek emergency care immediately.

Patient FAQ & Clinical Guidance

💡 What is the purpose of the TRAPPC11 gene test?

Snippet: This test detects disease‑causing variants in the TRAPPC11 gene to confirm autosomal recessive limb‑girdle muscular dystrophy type 2S.
يُكشف الاختبار عن الطفرات الجينية المسببة للحثل العضلي الطرفي المتنحي 2S لتأكيد التشخيص وتوجيه الرعاية.

💡 How is the sample collected and what preparation is needed?

Snippet: A simple blood draw or DNA FTA card sample is required; no fasting or medication discontinuation is necessary.
يُستخدم عينة دم أو بطاقة حفظ الحمض النووي دون حاجة للصيام أو إيقاف الأدوية.

💡 How should I interpret the result and what are the next steps?

Snippet: A positive result confirms the genetic basis of LGMD‑2S; a follow‑up with a clinical geneticist or neurologist is essential.
النتيجة الإيجابية تؤكد السبب الوراثي، ويتعين المتابعة مع أخصائي الوراثة السريرية أو طبيب الأعصاب.

UAE Regulatory & Accreditation Compliance

  • Licensed by DHA/MOHAP – Facility License: 9834453
  • ISO 9001:2015 Certified (Cert: INT/EGQ/2509DA/3139)
  • Data Privacy: Fully compliant with Federal Decree‑Law No. 41 of 2024 (Art. 87), Consent for Minors (CDS Law 2026), and UAE PDPL
  • All clinical recommendations align with 2026 DHA Guidelines and international genetic testing standards.

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