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2,800 AED

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DNAJC19 Gene Dilated Cardiomyopathy with Ataxia Genetic Test in UAE | 2800 AED | 2026 DHA Guidelines

تحليل جين DNAJC19 لتوسع عضلة القلب المصحوب بالرنح في الإمارات | 2800 درهم | معتمد من هيئة الصحة بدبي

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  • Premium Logistics: Paid Hospital-Grade Home Collection via ISO Certified Cold-Chain and VIP Mobile Phlebotomy (8 AM‑11 PM).
  • Clinical Guidance: Telephonic Post‑Test Clinical Guidance by DHA‑licensed specialists.
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يقدم هذا التحليل الجيني الدقيق رؤية شاملة لتشخيص اعتلال عضلة القلب التوسعي المصحوب بالرنح المرتبط بجين DNAJC19، وفق أعلى معايير الجودة المعتمدة في دولة الإمارات.

Clinical Overview

The DNAJC19 Gene Dilated Cardiomyopathy with Ataxia NGS Test screens the entire coding region of the DNAJC19 gene using Next‑Generation Sequencing, identifying pathogenic variants linked to 3‑methylglutaconic aciduria type V. This multisystem disorder manifests as infantile‑onset cardiomyopathy, ataxia, and growth failure. وفي الإمارات، يوفر هذا التحليل تشخيصًا دقيقًا للمرضى المعرضين لخطر اعتلال عضلة القلب والرنح، مما يوجه خطة العلاج والمتابعة السريرية.

Feature Our Test (DNAJC19 NGS) Closest Alternative
Technology Full gene NGS (Next Generation Sequencing) Targeted single‑gene Sanger sequencing
Coverage Complete coding region ±10 bp splice sites Limited to known hotspot mutations only
Turnaround Time 3–4 Weeks 4–6 Weeks
Clinical Sensitivity >99% for DNAJC19 variants ~80% (misses private mutations)
Regulatory Status DHA‑licensed, ISO 9001:2015, UAE PDPL compliant Non‑accredited international lab
Price 2800 AED 3200–4500 AED (variable)

Physician Insight & Safety Protocol

“A positive DNAJC19 result is not a standalone diagnosis – it must be correlated with clinical phenotype, imaging, and metabolic data. My advice: never interpret this test without expert genetic counselling, because the variant interpretation can change management significantly. Family cascade screening can be lifesaving.”

— Dr. PRABHAKAR REDDY, DHA License No. 61713011

⚠ Medication Warning

Do not discontinue prescribed medication without consulting your doctor. Cardiac medications (e.g., beta‑blockers, ACE inhibitors) must be managed by your cardiologist; sudden changes can precipitate acute heart failure.

🛑 Safety Exclusion Criteria & Emergency Signs

Exclusion Criteria:

  • Acute febrile illness or active infection
  • Sample not collected in DHA‑approved collection kit
  • Inability to obtain informed consent for genetic testing
  • Recent blood transfusion (<2 weeks)

ER Red Flags (seek immediate care):

  • New‑onset severe chest pain
  • Syncope (fainting) or sudden collapse
  • Palpitations with lightheadedness
  • Severe shortness of breath at rest

Patient FAQ & Clinical Guidance

1. What is the DNAJC19 gene test and how does it help?

Clinician’s Direct Answer: This uses next‑generation sequencing to detect pathogenic variants in DNAJC19, confirming a diagnosis of dilated cardiomyopathy with ataxia and guiding targeted treatment. يكشف هذا التحليل عن الطفرات الجينية المسؤولة عن المرض ويساعد في توجيه خطة علاجية شخصية.

2. Who should consider undergoing this genetic analysis?

Clinician’s Direct Answer: Individuals with unexplained dilated cardiomyopathy, ataxia, growth delay, or a family history of 3‑methylglutaconic aciduria should consider testing after formal genetic counselling. يُنصح بالتحليل للأشخاص الذين يعانون من أعراض قلبية عصبية مجهولة السبب أو تاريخ عائلي إيجابي.

3. How long does it take and what do results mean for my health?

Clinician’s Direct Answer: Results are reported within 3 to 4 weeks; a positive result indicates an increased risk for cardiomyopathy and ataxia, enabling early surveillance and family planning decisions. تظهر النتائج خلال ٣ إلى ٤ أسابيع، وتساعد في تحديد المخاطر المستقبلية ووضع خطة متابعة وقائية.

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