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Test Price

2,800 AED

✅ Home Collection Available

Test Name: SLC7A5 Gene (Phenylketonuria Modifier) | DNA Labs UAE

Executive Summary & Core Metrics

Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO‑accredited NGS processing.
Premium Logistics: VIP Mobile Phlebotomy & Temperature-Controlled Cold-Chain Home Collection (Available daily from 8 AM to 11 PM).
Clinical Guidance: Telephonic Post‑Test Clinical Guidance in result interpretation.
Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731.
Price: 2800 AED.

Test Overview & Methodology

This test screens the SLC7A5 gene, a well‑characterized modifier of phenylketonuria (PKU), using Next‑Generation Sequencing (NGS) to detect variants that can influence the severity of hyperphenylalaninemia. Understanding these genetic modifiers helps tailor dietary management and improve long‑term outcomes in affected individuals.

Feature Our Test – SLC7A5 NGS Closest Alternative – Standard PKU Panel
Gene Coverage Full SLC7A5 gene (coding & splicing regions) PAH gene only
Methodology Next‑Generation Sequencing (NGS) – Precision Standard NGS or limited Sanger sequencing
Turnaround Time 3–4 weeks 4–6 weeks
Price (AED) 2800 2500–3500

Physician Insight & Safety Protocols

Lina Osama Zaki Quteineh (DHA: 9294403): “The SLC7A5 gene test provides crucial information for customizing dietary management in phenylketonuria patients. Results must be integrated with clinical phenylalanine levels to avoid over‑ or under‑restriction. Our team offers detailed genetic counseling to help you apply these insights safely.”

Advisory for Safe Testing

Important Clinical Note

Do not alter any prescribed dietary formula or medication without consulting your specialist, as rapid changes may cause metabolic instability.

Safety Exclusion & Emergency Red Flags

  • Exclusion Criteria: Reschedule home collection if you have a fever, active infection, or have received a blood transfusion in the last 3 months.
  • ER Red Flags: Seek immediate care for symptoms such as confusion, severe headache, vomiting, seizures, or sudden behavioral changes—these may indicate acute hyperphenylalaninemia.

Patient FAQ & Clinical Guidance

1. What does SLC7A5 gene testing tell me about my PKU management?

This test identifies variants in the SLC7A5 gene that can modify the severity of phenylketonuria, directly influencing how strictly you must control dietary phenylalanine.

2. How soon can I expect results and what support do I get after?

Results are delivered within 3 to 4 weeks, accompanied by a telephonic session with a clinical geneticist to explain variant interpretation and next steps.

3. Is this test suitable for children and what are the legal requirements in the UAE?

Yes, the test is suitable for pediatric patients under UAE law, requiring documented parental consent and genetic counselling for minors.

UAE Regulatory & Data Privacy Adherence

Data Privacy: All genetic data is handled in strict 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. Medical liability is governed by Federal Decree-Law No. 4 of 2016 on Medical Liability.

Accreditation: ISO 9001:2015 Certified (Cert: INT/EGQ/2509DA/3139) | DHA-Licensed Facility (1143).

Clinical & Logistical Metadata

Test Name SLC7A5 Gene (Phenylketonuria Modifier) Genetic Test
Price (AED) 2800
Turnaround Time 3–4 weeks
Sample Type / Matrix Peripheral whole blood (EDTA) or extracted genomic DNA
Methodology Used Next-Generation Sequencing (NGS)
ICD-10-CM Code E70.0 (Classic Phenylketonuria)
LOINC Code 48508-4 (DNA probe)
DHA Facility License & Laboratory Address Invariants License No. 1143 | Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE

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