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2,800 AED

✅ Home Collection Available

AVPR2 Gene NSIAD Genetic Test in UAE | 2800 AED | 2026 DHA Guidelines

تحليل جين AVPR2 لمتلازمة الإفراز غير المناسب للهرمون المضاد لإدرار البول الكلوي المنشأ (NSIAD) في الإمارات | 2800 درهم | معتمد من هيئة الصحة بدبي

ضمان دقة تشخيصية بنسبة 99.9% عبر مختبر معتمد آيزو، مع خدمة سحب منزلي فاخرة واستشارة طبية هاتفية بعد النتيجة.

  • Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 Accredited Processing.
  • Premium Logistics: Paid Hospital-Grade Home Collection via ISO Certified Cold-Chain Home Collection.
  • VIP Mobile Phlebotomy: 8 AM to 11 PM, conducted by DHA-licensed phlebotomists.
  • Clinical Guidance: Telephonic Post-Test Clinical Guidance in result interpretation.
  • Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731.

Test Overview

This next-generation sequencing (NGS) test comprehensively screens the entire coding region of the AVPR2 gene to detect pathogenic variants responsible for nephrogenic syndrome of inappropriate antidiuresis (NSIAD), a rare X-linked disorder causing water retention and hyponatremia. يُستخدم هذا التحليل الجيني المتطور للكشف عن الطفرات المسببة لمرض نادر يؤثر على توازن الماء والصوديوم في الجسم.

Feature Our Test (AVPR2 NGS) Closest Alternative
Precision 99.9% analytical sensitivity & specificity ~95% (Sanger sequencing—limited variant detection)
Methodology NGS (Next Generation Sequencing) with full exon coverage and bioinformatics analysis Sanger sequencing (single-exon analysis)
Turnaround Time 3–4 weeks 4–6 weeks

Physician Insight & Safety Protocol

Dr. PRABHAKAR REDDY (DHA: 61713011): “A positive AVPR2 mutation confirms NSIAD, but clinical correlation with serum sodium, osmolality, and family history is essential to differentiate from SIADH or other hyponatremic states. This test empowers precise diagnosis and targeted management, avoiding unnecessary fluid restrictions or drug trials.”

⚠️ Medication Warning

Do not discontinue prescribed medication without consulting your doctor. Certain drugs (e.g., carbamazepine, SSRIs) can mimic or exacerbate hyponatremia; always inform your physician of all current therapies before testing.

Exclusion Criteria & Emergency Red Flags

  • Exclusion: Patients unable to provide a valid genetic counselling consent or with known interfering recent blood transfusion (<7 days).
  • Red Flag – Seek Immediate Medical Attention: Sudden severe headache, confusion, seizures, or altered consciousness—symptoms of acute hyponatremic encephalopathy.
  • Red Flag: Serum sodium <120 mmol/L or rapid drop >10 mmol/L in 24 hours requires urgent hospital evaluation.

Patient FAQ & Clinical Guidance

1. What exactly does the AVPR2 gene NSIAD NGS test detect, and who needs it?

This advanced next-generation sequencing test detects pathogenic variants in the AVPR2 gene causing nephrogenic syndrome of inappropriate antidiuresis, indicated for individuals with unexplained hyponatremia, low plasma osmolality, and normal adrenal/thyroid function. يُستخدم هذا الاختبار للمرضى الذين يعانون من نقص صوديوم الدم غير المفسر مع انخفاض الأسمولالية البلازمية واستبعاد الأسباب الأخرى.

2. How is the sample collected, and is home service available in the UAE?

A simple blood draw, extracted DNA, or a single drop of blood on an FTA card is collected via our ISO-certified home phlebotomy service, available 8 AM to 11 PM across all emirates. يتم جمع العينة عبر خدمة سحب الدم المنزلي المعتمدة آيزو والمتاحة من 8 صباحاً حتى 11 مساءً في جميع الإمارات.

3. What is the turnaround time, and does insurance cover the 2800 AED cost?

Results are delivered within 3 to 4 weeks at a fixed cost of 2800 AED, and we provide direct insurance billing verification via WhatsApp at +971 54 548 8731. تصدر النتائج خلال 3 إلى 4 أسابيع بسعر ثابت 2800 درهم، مع إمكانية التحقق من التغطية التأمينية عبر واتساب.

This complies with Federal Decree-Law No. 41 of 2024 (Art. 87) on Medical Laboratories, UAE CDS Law 2026 (genetic testing on minors requires guardian consent), and UAE PDPL data privacy regulations. Laboratory license: 9834453. ISO 9001:2015 Cert: INT/EGQ/2509DA/3139.

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