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Test Price

2,800 AED

✅ Home Collection Available

DCPS Gene Al-Raqad Syndrome Genetic Test in UAE | 2800 AED | 2026 DHA Guidelines

تحليل تسلسل الجينوم للجين DCPS لمتلازمة الرقاد في الإمارات | 2800 درهم | معتمد من هيئة الصحة بدبي

Executive Summary — 2026 E-E-A-T Compliant

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

الفحص الجيني NGS لمتلازمة الرقاد (جين DCPS) يقدم دقة تشخيصية 99.9% عبر معالجة معتمدة من ISO 9001:2015، مع خدمة سحب منزلي على مدار الساعة، وإرشاد سريري هاتفي بعد الفحص، وتسهيلات تأمين مباشر.

Test Overview & Methodology

This DNA test utilises Next-Generation Sequencing (NGS) to analyse the entire coding region of the DCPS gene, establishing a definitive diagnosis of Al-Raqad syndrome – a rare autosomal recessive neurodevelopmental disorder. يستخدم الفحص تقنية التسلسل الجيني من الجيل التالي (NGS) لتحليل جين DCPS المرتبط بمتلازمة الرقاد النادرة. A mandatory pre‑test genetic counselling session to draw a detailed pedigree chart is included; please provide complete clinical history of the affected individual.

Feature Our NGS Test (2800 AED) Standard Gene Panel (Alternative)
PrecisionFull DCPS gene sequencing with CNV detection (99.9% sensitivity)Limited to hotspot regions (~85% sensitivity)
MethodNGS + advanced bioinformatics, ISO-validated pipelineSanger sequencing or partial exons
Turnaround3–4 Weeks (ISO cold‑chain Courier)4–6 Weeks
Clinical SupportPre- & post-test DHA‑licensed genetic counsellingReport only

Clinical Guidance & Safety Protocol – Dr. Prabhakar Reddy (DHA: 61713011)

“As a DHA-licensed medical director, I emphasise that NGS results require expert correlation with clinical findings. This test provides high-resolution data, but a variant of uncertain significance must be interpreted within the patient's full phenotype and family history, in compliance with UAE Federal Decree‑Law No. 41 of 2024.”

Medication Warning

Do not discontinue prescribed medication without consulting your doctor. This genetic does not replace ongoing neurological or paediatric care.

Exclusion Criteria & Emergency Red Flags

  • Acute febrile illness (temperature >38.5°C) within 48 hours – reschedule home collection.
  • Severe dehydration or haemodynamic instability; go directly to the nearest emergency department.
  • Blood transfusion within the last 4 weeks – may compromise DNA extraction quality.
  • Any seizure activity within the past 2 hours – call 998 immediately.

If you experience respiratory distress, loss of consciousness, or uncontrolled seizures, do not wait for phlebotomy; call UAE Ambulance (998) immediately.

Regulatory & Data Privacy Compliance

Our services strictly follow Federal Decree‑Law No. 41 of 2024 (Art. 87) on medical laboratories, UAE CDS Law 2026 governing genetic testing of minors, and the UAE Personal Data Protection Law (PDPL). All genetic data is processed on encrypted servers within the UAE. Facility License: 9834453.

Frequently Asked Questions (FAQ)

What is the clinical utility of DCPS gene NGS testing for Al-Raqad syndrome?

A definitive molecular diagnosis of Al-Raqad syndrome via DCPS gene NGS guides prognosis, family planning, and targeted neurodevelopmental interventions. يوفر التشخيص الجزيئي لمتلازمة الرقاد عبر فحص جين DCPS توجيهًا دقيقًا للعلاج والتخطيط الأسري.

How is the sample collected and what are the logistic advantages in the UAE?

Our DHA‑licensed mobile phlebotomists perform pain‑free venous blood draw or accept dried blood spot (FTA card) at your doorstep, with cold‑chain transport ensuring sample integrity from collection to ISO lab in 60 minutes. يقوم فريق سحب الدم المرخص بزيارة منزلية سريعة وآمنة، مع نقل العينة بتبريد معياري خلال 60 دقيقة إلى المختبر المعتمد.

What do the results mean for my child’s long‑term health?

A pathogenic variant in DCPS confirms the syndrome, enabling multidisciplinary follow‑up with neurology, genetics, and early intervention services tailored to the 2026 DHA paediatric care pathways. يؤكد وجود طفرة مرضية في جين DCPS المتلازمة ويوجه خطة متابعة متعددة التخصصات مع أطباء الأعصاب والوراثة.

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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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