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Test Price

2,800 AED

✅ Home Collection Available

PRKAR1A Gene Myxoma, Intracardiac Genetic Test in UAE | 2800 AED | 2026 DHA Guidelines

تحليل جين PRKAR1A (الورم المخاطي داخل القلب) في الإمارات | 2800 درهم | معتمد من هيئة الصحة بدبي

Executive Summary

ملخص تنفيذي: اختبار جيني دقيق للكشف عن طفرات جين PRKAR1A المرتبطة بالورم المخاطي داخل القلب ومتلازمة كارني

  • 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.
  • Compliant with Federal Decree-Law No. 41 of 2024 (Art. 87), CDS Law 2026, and UAE PDPL.

Overview: PRKAR1A Genetic Testing for Intracardiac Myxoma

This next-generation sequencing (NGS) test fully analyses the PRKAR1A gene to detect pathogenic variants causing Carney complex and intracardiac myxoma, delivering clinical-grade precision and risk stratification. يُحلل هذا الاختبار جين PRKAR1A بالكامل لتحديد الطفرات المسببة للأورام المخاطية داخل القلب بدقة تشخيصية عالية.

Feature Our Test (NGS Pan‑Gene Analysis) Closest Alternative (Sanger Sequencing)
Methodology Next‑Generation Sequencing (NGS) – full gene coverage Sanger sequencing – limited to known hotspots
Diagnostic Sensitivity >99.9% for single‑nucleotide variants and indels ~95% for targeted regions only
Turnaround Time 3–4 Weeks 2–4 Weeks
ISO 9001:2015 Certified Yes (Cert: INT/EGQ/2509DA/3139) Often not guaranteed

Physician Insight & Patient Safety Protocol

“As a DHA-licensed clinical pathologist, I emphasize that this test must be correlated with clinical imaging, cardiologic evaluation, and detailed family history. Genetic findings guide surveillance—they never replace clinical judgement. Do not alter any prescribed therapy without direct medical consultation.”

– Dr. Prabhakar Reddy, DHA License: 61713011

⚠ Important: Do not discontinue prescribed medication without consulting your doctor.

Exclusion Criteria & Emergency Red Flags

  • Individuals unable to provide informed consent; minors require legal guardian consent per UAE CDS Law 2026.
  • Known pregnancy is not a contraindication, but clinical interpretation may need adjustment; discuss with your physician.
  • Emergency Red Flags:
  • Chest pain, palpitations, transient ischemic attack, or sudden neurological deficits — seek immediate emergency care.

Frequently Asked Questions (Patient Guidance)

What does the PRKAR1A gene test detect, and why is it critical for cardiac myxoma?

The PRKAR1A NGS test identifies pathogenic mutations in the PRKAR1A gene linked to Carney complex and intracardiac myxoma, enabling precise risk stratification, early surveillance, and informed family counselling. يكتشف تحليل جين PRKAR1A الطفرات المرتبطة بالورم المخاطي داخل القلب ومتلازمة كارني، مما يتيح الكشف المبكر والاستشارة الوراثية.

How is the sample collected, and what is the turnaround time?

A whole blood, extracted DNA, or a dried blood spot on an FTA card is collected via our cold-chain home service, with results reported within 3 to 4 weeks using ISO‑certified NGS. تُجمع العينة عبر خدمة منزلية موثوقة، وتظهر النتائج خلال 3 إلى 4 أسابيع باستخدام التسلسل الجيني المتطور.

Is this covered by UAE health insurance, and how can I verify?

Many UAE insurance plans cover genetic testing for clinical suspicion of Carney complex; we provide direct billing verification via WhatsApp at +971 54 548 8731 before sample collection. تُغطي العديد من خطط التأمين في الإمارات هذا الفحص الجيني عند الشك السريري؛ تحقق من تغطيتك عبر واتساب.

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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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