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Test Price

2,000 AED

✅ Home Collection Available

Targeted Mutation Analysis (2 Mutations) in UAE | 2000 AED

Trust Grade A ISO 9001:2015 DHA Licensed
DHA
MOHAP
APPROVED

Executive Summary & Core Metrics

Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO Accredited Processing.
Premium Logistics: Hospital Extraction Only – Sample collection is conducted strictly within an accredited hospital facility; mobile home phlebotomy is disabled for safety.
Clinical Guidance: Telephonic Post-Test Clinical Guidance in result interpretation by DHA-licensed genetic counsellors.
Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731 – instant confirmation before collection.

Test Overview & Methodology

Targeted Mutation Analysis (2 Mutations) identifies two precisely designated gene variants using the gold‑standard Sanger sequencing method, providing definitive answers for hereditary cancer syndromes, prenatal diagnosis, and rheumatologic predisposition.

Feature Our UAE Advanced Test Closest Alternative
Methodology Sanger Sequencing (Gold Standard, single‑base resolution) NGS panels (lower per‑variant depth)
Diagnostic Sensitivity 99.9% for targeted mutations 89–95% (may miss rare SNVs)
Turnaround Time 10–15 days from collection 3–4 weeks
Sample Types Peripheral blood, plasma, serum, amniotic fluid, cord blood, chorionic villi Often limited to blood/saliva
Accreditation ISO 9001:2015 (Cert: INT/EGQ/2509DA/3139), DHA‑MOHAP licensed Varies, may be unaccredited

Physician Insight & Safety Protocols

A note from Lina Osama Zaki Quteineh, Consultant Medical Genetics (DHA Registration ID: 9294403)

“While this targeted analysis delivers near‑absolute certainty for the two mutations tested, it must be interpreted within your full clinical and family history. A negative result does not eliminate all genetic risk, and a positive finding should be discussed with a specialised physician to plan preventive or therapeutic steps.”

“I urge every patient to remember that no laboratory result replaces a comprehensive consultation—correlate these findings with imaging, physical examination, and personal health context.”

Medication Advisory

Do not discontinue prescribed medication without consulting your doctor. Genetic test preparation may require temporary pausing of certain supplements; always follow your physician's advice.

Exclusion Criteria & Emergency Red Flags

Exclusion Criteria:

  • Active chemotherapy or radiotherapy (must wait 4 weeks post‑treatment)
  • Recent blood transfusion (< 2 weeks prior)
  • Acute infection with high fever
  • Known interfering anticoagulants not suspended (per physician guidance)

Seek Immediate Medical Care if:

  • Severe bleeding or hematoma at collection site
  • Signs of amniotic fluid leakage after invasive prenatal sampling
  • Fever > 38.5°C post amniocentesis
  • Sudden vision changes or numbness (rare embolic event)

Patient FAQ & Clinical Guidance

1. What exactly does Targeted Mutation Analysis (2 Mutations) detect and how reliable is it?

It detects the presence or absence of two specific DNA sequence variants using Sanger sequencing, delivering 99.9% analytical sensitivity and specificity.

2. Which specialists typically order this test and for what conditions?

Gynecologists, oncologists, and rheumatologists request it for hereditary breast/ovarian cancer syndromes, prenatal diagnosis, and genetic rheumatic disorders.

3. How is the sample collected and when will I receive my results?

A blood draw, amniotic fluid, or cord blood sample is taken within a hospital setting; results are securely delivered within 10–15 days via encrypted digital report.

4. Can I get this test done at home?

No. Because the specimen types include invasive prenatal fluids and cord blood, collection is strictly hospital-based for safety and clinical oversight.

UAE Regulatory & Data Privacy Adherence

  • Federal Decree-Law No. 45 of 2021 on Personal Data Protection (PDPL): Genomic data processed under strict data‑protection protocols; reports transmitted only via encrypted channels.
  • Federal Law No. 2 of 2019 Concerning the Use of Information and Communication Technology in Health Fields: All electronic health data handling and telephonic guidance comply with mandated security standards.
  • Federal Decree-Law No. 4 of 2016 on Medical Liability: Clinical testing safety and patient consent requirements are fully observed.
  • ISO 9001:2015 (Cert: INT/EGQ/2509DA/3139): Quality management across all pre‑analytical, analytical and post‑analytical phases.

Clinical & Logistical Metadata

Test Name Targeted Mutation Analysis (2 Mutations)
Price (AED) 2,000 AED
Turnaround Time 10–15 days from receipt at the ISO‑certified laboratory
Sample Type / Matrix Peripheral blood, plasma, serum, amniotic fluid, cord blood, chorionic villi
Methodology Used Sanger Sequencing (Gold Standard, single‑base resolution)
ICD-10-CM Code Z13.89 (Encounter for screening for other specified genetic and chromosomal disorders)
LOINC Code 81263-9 (Targeted mutation analysis in Blood or Tissue by Sequencing)
DHA Facility License & Address License No. 1143 | Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE

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