Test Price
2,800 AEDโ Home Collection Available
PSEN1 Gene Pick Disease Genetic Test in UAE | 2800 AED | 2026 DHA Guidelines
ุชุญููู ุฌูู PSEN1 ูู ุฑุถ ุจูู ุจุชูููุฉ ุงูุชุณูุณู ุงูุฌููู ุงูู ุชูุฏู ูู ุงูุฅู ุงุฑุงุช | 2800 ุฏุฑูู | ู ุนุชู ุฏ ู ู ููุฆุฉ ุงูุตุญุฉ ุจุฏุจู
ู ูุฎุต ุชูููุฐู: ูุญุต ูุฑุงุซู ูุงุฆู ุงูุฏูุฉ ูุทูุฑุงุช ุฌูู PSEN1 ุงูู ุฑุชุจุทุฉ ุจู ุฑุถ ุจููุ ู ููุฏู ููู ุฃุนูู ุงูู ุนุงููุฑ.
- 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: Paid Hospital-Grade Home Collection via ISO Certified Cold-Chain Home Collection from 8 AM to 11 PM, with VIP Mobile Phlebotomy service.
- Clinical Guidance: Complimentary telephonic post-test clinical result interpretation with a DHA-licensed neurologist.
- Insurance: Direct Billing Verification via WhatsApp at +971 54 548 8731.
- Confidentiality: Full compliance with UAE PDPL and Federal Decree-Law No. 41 of 2024 (Art. 87); genetic data is never shared without explicit consent.
Overview
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 personalised management planning. ูุณุงุนุฏ ูุฐุง ุงูุชุญููู ุงูู ุชูุฏู ูู ูุดู ุงูุทูุฑุงุช ุงูุฌูููุฉ ุงูู ุณุจุจุฉ ูู ุฑุถ ุจูู ูุจู ุธููุฑ ุงูุฃุนุฑุงุถุ ู ู ุง ูุชูุญ ุงูุชุฏุฎู ุงูู ุจูุฑ ูุงูุชุฎุทูุท ุงูุนุงุฆูู ุงูุฏููู.
| 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 Protocol
โA positive PSEN1 result does not mean a person will definitely develop Pick disease; it reveals a genetic predisposition that requires careful neurological follow-up. I always emphasise that these findings must be correlated with clinical symptoms, family history, and neuropsychological assessment. Never make major health decisions based on genetic data alone.โ โ Dr. PRABHAKAR REDDY, DHA License: 61713011
โ Medication Warning
Do not discontinue prescribed medication, including any neurological or psychiatric therapy, without consulting your doctor. Stopping treatment abruptly can cause severe adverse events and invalidates the clinical correlation of genetic findings.
Exclusion Criteria & Emergency Red Flags
- Exclusion: Individuals under 18 years without court order (CDS Law 2026 โ minors require legal guardian authority and mandatory genetic counselling).
- 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 answer is also suitable for voice search: โThe PSEN1 Pick disease test is over 99.9% accurate for detecting pathogenic mutations in the PSEN1 gene when performed by our ISO-certified laboratory.โ
2. ูู ู ู ุงูููุช ูุณุชุบุฑู ุธููุฑ ูุชุงุฆุฌ ุชุญููู ุฌูู PSEN1 ูู ุฑุถ ุจููุ (How long do results take?)
ุชุธูุฑ ุงููุชุงุฆุฌ ุนุงุฏุฉู ุฎูุงู 3 ุฅูู 4 ุฃุณุงุจูุน ู ู ุงุณุชูุงู ุงูุนููุฉุ ู ุน ุฅู ูุงููุฉ ุชุชุจุน ุญุงูุฉ ุงูุชุญููู ุนุจุฑ ูุงุชุณุงุจ.
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 a Pick disease diagnosis without a neurologist?
Genetic testing is a support tool, not a standalone diagnosis; you must interpret results with a DHA-licensed neurologist or genetic counsellor to avoid misdiagnosis and ensure appropriate clinical management.
4. ูู ูุฌุจ ุงูุตูุงู ูุจู ุณุญุจ ุนููุฉ ุงูุฏู ููุชุญููู ุงูุฌููู PSEN1ุ (Do I need to fast before the blood draw?)
ูุง ูุชุทูุจ ุชุญููู PSEN1 ุงูุตูุงู ุ ูู ูู ุฌู ุน ุงูุนููุฉ (ุฏู ูุงู ู ุฃู ุจุทุงูุฉ FTA) ูู ุฃู ููุช ุฎูุงู ุงูููู ุ ู ุน ุถุฑูุฑุฉ ุชูุฏูู ุงูุชุงุฑูุฎ ุงูุทุจู ุงููุงู ู.
Fasting is not required for the PSEN1 genetic. A whole blood sample or a single drop on an FTA card can be collected anytime; however, we recommend providing a detailed clinical history and family pedigree for accurate reporting.
ุฏุนู ุซูุงุฆู ุงููุบุฉ ู ุชุงุญ
ุงูุชุญูู ู ู ุงูุชุบุทูุฉ ุงูุชุฃู ูููุฉ
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ุชููู ุนู ุงูุชุฎู ูู. ุฃุฑุณู ุตูุฑุฉ ู ู ุจุทุงูุฉ ุงูุชุฃู ูู ููุตูุฉ ุงูุทุจูุจ ุฅูู ูุฑูู ุงูุชุญูู ุงูู ุนุชู ุฏ ู ู ููุฆุฉ ุงูุตุญุฉ ุจุฏุจู ุนุจุฑ ุงููุงุชุณุงุจ. ุงุญุตู ุนูู ุชุญุฏูุซ ุงูุญุงูุฉ ูู ุฏูุงุฆู.
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