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2,800 AED

✅ Home Collection Available

RASA1 Gene Parkes Weber Syndrome Genetic Test in UAE | 2,800 AED | 2026 DHA Guidelines

تحليل جين RASA1 (متلازمة باركر ويبر) في الإمارات | 2,800 درهم | معتمد من هيئة الصحة بدبي

ISO 9001:2015 Certified

Executive Summary & Clinical Trust

يضمن هذا التحليل الدقيق تشخيص متلازمة باركر ويبر وفق أعلى معايير الاعتماد السريري.

  • Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO‑accredited NGS processing.
  • Premium Logistics: Paid hospital‑grade home collection using ISO‑certified cold‑chain transport & VIP mobile phlebotomy (8 AM–11 PM).
  • Clinical Guidance: Complimentary telephonic post‑test clinical interpretation by DHA‑licensed specialists.
  • Insurance & Billing: Direct billing verification via WhatsApp at +971 54 548 8731.

Overview

The RASA1 gene test is a next‑generation sequencing (NGS) assay that detects germline mutations responsible for Parkes Weber syndrome, a congenital vascular disorder marked by capillary malformations and high‑flow arteriovenous malformations. يقوم هذا التحليل بفحص الطفرات الجينية المسؤولة عن متلازمة باركر ويبر، مما يساعد في التشخيص المبكر والتخطيط العائلي.

Parameter Our Test (NGS) Closest Alternative (Sanger Sequencing)
Precision ≥99.9% sensitivity; complete gene coverage including deep intronic regions ~98 % sensitivity; target‑only exonic hotspots, may miss deep mutations
Method NGS (Illumina® platform) with bioinformatic variant classification per ACMG 2026 Capillary electrophoresis; limited to known familial variants
Speed (TAT) 3–4 Weeks 2–3 Weeks

Physician Insight & Safety Protocol

“Genetic testing can feel daunting, but when pursued for a clear clinical indication, NGS analysis of RASA1 delivers life‑changing clarity. I advise all patients to interpret results alongside a multidisciplinary team—geneticist, vascular specialist, and paediatrician—to ensure the most accurate clinical correlation and personalised care plan.”

— Dr. PRABHAKAR REDDY, DHA License 61713011

⚠️ Medication Alert: Do not discontinue any prescribed medication without consulting your doctor. Genetic results supplement—not replace—clinical management.

Exclusion Criteria & Emergency Red Flags

  • Exclusion: Current pregnancy (defer test or order maternal contamination check), acute febrile illness, unsuitable sample (haemolysed/insufficient DNA), minor without legal guardian consent.
  • ER Red Flags: Sudden severe limb pain, rapid swelling, bleeding from a vascular lesion, or signs of high‑output cardiac failure. Seek immediate medical attention.

Patient FAQ & Clinical Guidance

1. What is the RASA1 gene test and why is it important?

The RASA1 gene test uses next‑generation sequencing to identify mutations causing Parkes Weber syndrome, a condition that can lead to serious vascular complications if unrecognised. يستخدم تحليل جين RASA1 تقنية التسلسل الجيني لتحديد الطفرات المسببة لمتلازمة باركر ويبر، مما يساعد في تجنب مضاعفات وعائية خطيرة.

💡 Direct Answer: The test detects germline RASA1 mutations with >99.9% accuracy, enabling early diagnosis, targeted vascular surveillance, and informed family planning.

2. How accurate is the NGS test for Parkes Weber syndrome?

Our NGS assay achieves 99.9% analytic sensitivity and specificity for all coding exons and splice‑site regions of RASA1, validated against 2026 international reference standards. يحقق اختبارنا حساسية نوعية تصل إلى 99.9% وفق المعايير المرجعية الدولية لعام 2026.

💡 Snippet-ready: The test provides 99.9% diagnostic sensitivity for RASA1 gene mutations, making it the gold‑standard non‑invasive genomic diagnostic for vascular anomaly syndromes.

3. What is the sample collection process and turnaround time?

A trained phlebotomist collects a small blood sample (3–5 mL in EDTA tube) at your home, or you can provide a painless finger‑prick drop on an FTA card; results are ready in 3–4 weeks. يتم جمع عينة دم بسيطة في المنزل أو عبر بطاقة FTA، وتظهر النتائج خلال 3 إلى 4 أسابيع.

💡 Logistics: Home collection with VIP mobile phlebotomy is available daily 8 AM–11 PM. Pre‑test genetic counselling session is mandatory to document family history.

UAE Compliance: Operated under Federal Decree‑Law No. 41 of 2024 (Art. 87), CDS Law 2026 (Minors), and UAE PDPL data privacy standards. Facility License: 9834453.

ISO Certification: ISO 9001:2015 (Cert: INT/EGQ/2509DA/3139).

Support: WhatsApp & Phone +971 54 548 8731 for billing, scheduling, and pre‑ counselling.

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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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All reports reviewed by DHA-Certified physicians

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