Test Price
2,800 AEDโ Home Collection Available
PSEN1 Gene Pick Disease Genetic Test in UAE | 2800 AED | DHA Licensed Lab 1143
Executive Summary & Core Metrics
High-Precision Genetic Screening for PSEN1 Mutations Linked to Pick Disease
- Accuracy Guarantee: 99.9% diagnostic sensitivity via ISO 9001:2015 certified processing (Cert: INT/EGQ/2509DA/3139) using advanced Next-Generation Sequencing (NGS).
- Premium Logistics: VIP Mobile Phlebotomy and temperature-controlled cold-chain home collection available daily from 8 AM to 11 PM.
- Clinical Guidance: Complimentary telephonic post-test result interpretation with a DHA-licensed Consultant Medical Geneticist.
- Insurance: Direct billing verification via WhatsApp at +971 54 548 8731.
- Confidentiality: Full compliance with Federal Decree-Law No. 45 of 2021 on Personal Data Protection (PDPL) and Federal Law No. 2 of 2019 Concerning the Use of Information and Communication Technology in Health Fields. Genetic data is never shared without explicit consent.
Test Overview & Methodology
The PSEN1 Gene Pick Disease Genetic Test screens for pathogenic variants in the PSEN1 gene associated with autosomal dominant Pick disease and related frontotemporal dementia (FTD). This test utilizes Next-Generation Sequencing to analyze coding exons and splice sites, delivering a report that supports early diagnosis, family risk assessment, and personalized management planning. Early detection of PSEN1 mutations enables proactive neurological monitoring and informed family counseling.
| Feature | Our Test (NGS) | Closest Alternative (Sanger Sequencing) |
|---|---|---|
| Precision | 99.9% analytical sensitivity | ~99.0% for single variant |
| Method | Massively parallel NGS with full exon coverage | Sequential Sanger; limited to known hotspots |
| Turnaround | 3 โ 4 Weeks with ISO cold chain | 5 โ 7 Weeks (fragmented workflow) |
Physician Insight & Safety Protocols
โA positive PSEN1 result indicates a genetic predisposition for Pick disease, but it does not confirm that symptoms will manifest. Clinical correlation with neurological examination, family history, and neuropsychological assessment remains essential. I advise patients to avoid making major health decisions based solely on genetic data and to seek multidisciplinary evaluation.โ โ Lina Osama Zaki Quteineh, Consultant Medical Genetics, DHA Registration ID: 9294403
Advisory โ Medication Continuation
Continue all prescribed neurological or psychiatric medications unless your treating physician expressly advises otherwise. Abrupt discontinuation may lead to serious adverse events and can confound the clinical interpretation of genetic findings.
Exclusion Criteria & Emergency Red Flags
- Exclusion: Individuals under 18 years without a court order โ minors require legal guardian authority and mandatory genetic counselling under Federal Decree-Law No. 4 of 2016 on Medical Liability.
- Exclusion: Patients unable to provide informed consent or without a legal representative.
- ER Red Flag: Sudden onset of confusion, seizures, or stroke-like symptoms while awaiting results โ seek emergency care immediately; genetic testing does not replace urgent clinical assessment.
- Safety: Home collection is contraindicated in cases of active bleeding disorders; please contact our medical team for alternative arrangements.
Patient FAQ & Clinical Guidance
1. How accurate is the PSEN1 Pick disease genetic test?
Our NGS test identifies single nucleotide variants and small insertions/deletions in the PSEN1 gene with >99.9% analytical sensitivity and specificity, making it the most reliable genetic screening tool for Pick disease in the UAE. The test is performed in our ISO 9001:2015 certified laboratory.
2. How long does it take to get results?
Results are typically available within 3 to 4 weeks from sample accession. We provide a WhatsApp tracking link so you can follow your sampleโs progress securely.
3. Can I use this test to confirm Pick disease without seeing a neurologist?
Genetic testing is a supportive tool, not a standalone diagnosis. Results must be interpreted by a DHA-licensed Consultant Medical Geneticist or neurologist to avoid misdiagnosis and ensure appropriate clinical management.
4. Do I need to fast before the blood draw for PSEN1 genetic testing?
Fasting is not required for the PSEN1 genetic test. A whole blood sample or a single drop on an FTA card can be collected at any time. We recommend providing a detailed clinical history and family pedigree for accurate reporting.
UAE Regulatory & Data Privacy Adherence
Data Protection & Health Information Governance
This genetic testing service operates in full compliance with Federal Decree-Law No. 45 of 2021 on Personal Data Protection (PDPL) and Federal Law No. 2 of 2019 Concerning the Use of Information and Communication Technology in Health Fields. All genetic data is encrypted, access-controlled, and never shared with third parties without your explicit written consent. Clinical safety and patient consent procedures adhere to Federal Decree-Law No. 4 of 2016 on Medical Liability. Your privacy and data sovereignty are protected under UAE law.
Clinical & Logistical Metadata
| Test Name | PSEN1 Gene Sequencing for Pick Disease (Frontotemporal Dementia) |
| Price (AED) | 2,800 AED |
| Turnaround Time | 3 โ 4 Weeks |
| Sample Type / Matrix | Whole Blood (EDTA) or FTA Card โ VIP Mobile Phlebotomy & Temperature-Controlled Cold-Chain Home Collection available daily 8 AM โ 11 PM |
| Methodology Used | Next-Generation Sequencing (NGS) โ Full coding exon and splice site coverage |
| ICD-10-CM Code | G31.01 (Pick disease) |
| LOINC Code | 21636-6 (Gene mutations identified in Blood or Tissue by Sequencing) |
| DHA Facility License & Laboratory Address | DHA License No: 1143 | Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE | DNA Labs UAE |
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