Test Price
2,800 AED✅ Home Collection Available
GLUL Gene Glutamine Deficiency, Congenital – Genetic Test in UAE | 2800 AED | DHA Approved
Executive Summary & Core Metrics
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO Accredited Next-Generation Sequencing.
- Premium Logistics: VIP Mobile Phlebotomy & Temperature-Controlled Cold-Chain Home Collection (Daily 8 AM – 11 PM).
- Clinical Guidance: Telephonic post-test clinical guidance for result interpretation and management planning.
- Insurance: Direct billing verification via WhatsApp +971 54 548 8731.
Test Overview & Methodology
The GLUL Gene NGS Test identifies pathogenic variants in the GLUL gene causing congenital glutamine synthetase deficiency, a severe inborn error of metabolism. This advanced genetic analysis provides definitive diagnosis for symptomatic infants and children, guiding life-saving dietary and medical interventions.
| Feature | Our Test (NGS) | Closest Alternative (Biochemical) |
|---|---|---|
| Methodology | Next-Generation Sequencing (Whole Gene) | Enzymatic / Metabolite Assay |
| Precision | 99.9% Analytical Sensitivity | Variable, Qualitative |
| Turnaround Time | 15–21 Business Days | 5–7 Business Days |
| Clinical Utility | Gold-standard: mutation identification, carrier testing, prenatal diagnosis | Screening only; cannot confirm genetic cause |
Physician Insight & Safety Protocols
Consultant Medical Genetics – Lina Osama Zaki Quteineh | DHA ID: 9294403
"Congenital glutamine synthetase deficiency is a rare but life-altering condition. The NGS test provides a definitive molecular diagnosis, enabling timely interventions such as specific dietary adjustments and anticonvulsant therapies. However, results must always be correlated with clinical presentation, metabolic profiles, and imaging. Our multidisciplinary team ensures comprehensive pre- and post-test counseling for families."
⚠️ Medication Advisory
Do not discontinue or alter any prescribed medications without consulting the managing physician. Genetic testing does not replace ongoing clinical management or medication adjustments. Always follow your healthcare provider’s instructions for anticonvulsants, dietary supplements, and metabolic therapies.
Exclusion Criteria & ER Red Flags
- Patients with active severe infection or who are immunocompromised should consult their physician before sample collection.
- Newborns must be clinically stable; immediate emergency care overrides genetic testing.
- ER Red Flags: If the individual develops acute vomiting, lethargy, seizures, or respiratory distress, seek emergency medical attention immediately—do not wait for test results.
Patient FAQ & Clinical Guidance
1. What is the GLUL NGS test and why is it ordered?
This test detects mutations in the GLUL gene responsible for congenital glutamine synthetase deficiency. It is ordered for infants presenting with unexplained seizures, developmental delay, metabolic acidosis, or other symptoms suggestive of an inborn error of metabolism. It is also used for carrier testing in at-risk family members and for prenatal diagnosis.
2. How accurate is genetic testing compared to traditional biochemical methods?
NGS offers 99.9% analytical sensitivity for detecting single-nucleotide variants and small insertions/deletions. Unlike enzymatic or metabolite assays, which may give false positives or negatives, NGS provides a definitive molecular diagnosis, reducing diagnostic delay and enabling precise therapeutic targeting.
3. Is home sample collection available and safe for my child?
Yes, we offer hospital-grade home collection by licensed pediatric phlebotomists following strict cold-chain protocols. Pain-minimizing techniques are used for infants and children. The sample is transported directly to our ISO-accredited laboratory, ensuring specimen integrity and rapid processing. Service hours are daily 8 AM – 11 PM.
UAE Regulatory & Data Privacy Adherence
This service complies with Federal Decree-Law No. 45 of 2021 on Personal Data Protection (PDPL), Federal Law No. 2 of 2019 Concerning the Use of Information and Communication Technology in Health Fields, and Federal Decree-Law No. 4 of 2016 on Medical Liability. All genetic data is handled with strict confidentiality and stored securely. Laboratory certification: ISO 9001:2015 (Cert: INT/EGQ/2509DA/3139).
Clinical & Logistical Metadata
| Test Name | GLUL Gene Glutamine Deficiency, Congenital – Genetic Test (NGS) |
| Price (AED) | 2,800 AED |
| Turnaround Time | 15–21 Business Days |
| Sample Type / Matrix | Peripheral Blood (Whole Blood – EDTA) – VIP Mobile Phlebotomy & Temperature-Controlled Cold-Chain Home Collection available daily 8 AM–11 PM |
| Methodology Used | Next-Generation Sequencing (Panel-based whole gene sequencing) |
| ICD-10-CM Code | E72.24 (Congenital glutamine synthetase deficiency) |
| LOINC Code | 88990-2 (GLUL gene mutation detection) |
| DHA Facility License & Laboratory Address | License No: 1143 | Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE | DNA Labs UAE |
دعم ثنائي اللغة متاح
التحقق من التغطية التأمينية
Check Insurance Coverage Instantly
Stop the guesswork. Send a photo of your Insurance Card and Doctor's Prescription to our DHA-Certified Verification Team on WhatsApp.
توقف عن التخمين. أرسل صورة من بطاقة التأمين ووصفة الطبيب إلى فريق التحقق المعتمد من هيئة الصحة بدبي عبر الواتساب. احصل على تحديث الحالة في دقائق.
Available in Arabic, English, Hindi & Urdu
ISMS 27001:2022
ISO Accredited
HIPAA
All reports reviewed by DHA-Certified physicians