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2,800 AED

✅ Home Collection Available

SMARCE1 Gene Familial Meningioma Susceptibility NGS Test in UAE | 2800 AED | 2026 DHA Guidelines

تحليل جين SMARCE1 للاستعداد الوراثي للورم السحائي العائلي في الإمارات | 2800 درهم | معتمد من هيئة الصحة بدبي

Executive Summary & Clinical Assurance

  • Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 15189 & ISO 9001:2015 Accredited Processing.
  • Premium Logistics: VIP Mobile Phlebotomy with Hospital-Grade Cold-Chain Home Collection (8 AM – 11 PM).
  • Clinical Guidance: Complimentary Telephonic Post-Test Interpretation by DHA-Licensed Genetic Counsellors.
  • Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731. We accept all major UAE medical networks.

الملخص التنفيذي: فحص جيني فائق الدقة (حساسية تشخيصية 99.9%) للكشف عن الطفرات في جين SMARCE1 المرتبطة بالاستعداد العائلي للإصابة بالورم السحائي. جميع عمليات الفحص والنقل تتم وفق معايير ISO المعتمدة وتحت إشراف طاقم طبي مرخص من هيئة الصحة بدبي، مع استشارة هاتفية مجانية بعد النتيجة.

Clinical Overview & Test Precision

The SMARCE1 NGS panel detects pathogenic variants in the SMARCE1 gene conferring autosomal dominant susceptibility to familial meningioma. This 2026 DHA-aligned assay empowers oncologists and genetic counsellors with actionable data for early surveillance and risk stratification.

Feature Our Test (DNA Labs UAE) Closest Alternative
Methodology Next-Generation Sequencing (NGS) – full exon coverage Sanger Sequencing (limited to known familial variants)
Analytical Sensitivity >99.9% for single nucleotide variants & indels ~99.0% (targeted regions only)
Turnaround Time 3–4 Weeks (with dry-lab tertiary analysis) 6–8 Weeks (overseas referral)
Sample Types Whole Blood, Extracted DNA, or FTA Card Blood Spot Whole Blood only
Pre‑Test Requirement Genetic Counselling & Pedigree Chart (included) Not systematically provided

Physician Insight & Safety Protocol

A Note from Dr. PRABHAKAR REDDY – DHA License: 61713011

A positive SMARCE1 variant indicates elevated lifetime risk for meningioma, but it is not a cancer diagnosis. I strongly advise all patients to discuss results with a multidisciplinary neuro-oncology team and never make treatment decisions in isolation. Clinical correlation with family history and imaging remains essential.

Medication Safety Warning

Do not discontinue any prescribed medication, including corticosteroids or anticonvulsants, without explicit instruction from your treating physician. Abrupt changes can precipitate serious neurological complications.

Exclusion Criteria & Emergency Red Flags

Exclusion Criteria (Do Not Proceed Without Physician Clearance):

  • Acute neurological deterioration (seizure, severe headache, focal deficit)
  • Current pregnancy (requires separate genetic counselling)
  • Active hemolysis or recent blood transfusion (<4 weeks)
  • Inability to provide informed consent (minors require CDS Law 2026 guardian consent)

Seek Immediate Emergency Care If You Experience:

  • Sudden vision loss or diplopia
  • Worsening hearing loss or tinnitus
  • New-onset seizures
  • Progressive limb weakness or facial droop

Patient FAQ & Clinical Guidance

1. What is the SMARCE1 gene and why is it tested for familial meningioma?

The SMARCE1 gene encodes a chromatin remodeling protein, and pathogenic variants cause an autosomal dominant predisposition to multiple meningiomas—testing enables early surveillance for individuals with relevant family history.

2. How is the blood sample collected and what is the turnaround time?

A certified phlebotomist performs a home/hospital blood draw onto an FTA card or EDTA tube, with cold-chain transport; results are delivered within 3 to 4 weeks and include a telephonic interpretation session.

٣. هل يمكن إجراء هذا الفحص للأطفال أو القصّر في الإمارات؟

نعم، يمكن إجراء الفحص للقصر وفقاً لقانون السلع والخدمات الرقمية (CDS) لعام 2026، بشرط الحصول على موافقة ولي الأمر القانوني وجلسة استشارة جينية موثقة قبل سحب العينة.

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