Test Price
2,800 AEDโ Home Collection Available
GPD1 Gene Sequencing for Transient Infantile Hypertriglyceridemia in UAE โ 2,800 AED
Executive Summary & Core Metrics
Accuracy Guarantee: 99.9% diagnostic sensitivity via ISO 9001:2015 accredited NGS processing for complete GPD1 gene coverage.
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 by a DHA-licensed Consultant Medical Genetics specialist.
Insurance Verification: Direct billing pre-verification via WhatsApp at +971 54 548 8731.
Test Overview & Methodology
This definitive Next-Generation Sequencing (NGS) assay analyzes the entire coding region of the GPD1 gene to diagnose Transient Infantile Hypertriglyceridemia (HTGTI), a rare autosomal recessive disorder that presents with severe hypertriglyceridemia in infancy and typically resolves spontaneously. The test is indicated for neonates and infants with unexplained elevated triglycerides, helping clinicians differentiate a primary genetic etiology from secondary causes and guiding precise dietary management to prevent pancreatitis.
Comparative Diagnostic Value
| Feature | Our GPD1 NGS Test | Standard Lipid Panel |
|---|---|---|
| Diagnostic Precision | >99.9% sensitivity for GPD1 pathogenic variants | Non-specific; cannot confirm genetic cause |
| Methodology | Next-Generation Sequencing (full gene coverage) | Enzymatic colorimetric assay |
| Turnaround Time | 3โ4 weeks (definitive molecular diagnosis) | 24โ48 hours (lipid levels only) |
| Clinical Actionability | Enables targeted family screening and personalized follow-up | Requires further genetic testing for etiology |
Physician Insight & Safety Protocols
โA positive GPD1 variant must be interpreted alongside the infantโs clinical history and serial lipid profiles. Genetic findings alone do not replace bedside judgment. Our DHA-licensed team provides a dedicated post-test consultation to ensure families understand dietary recommendations and long-term surveillance needs.โ
โ Lina Osama Zaki Quteineh, Consultant Medical Genetics, DHA Registration ID: 9294403
Advisory โ Medication Continuity
Do not discontinue any prescribed lipid-lowering or anticoagulant medication without consulting your treating physician. All testing and therapeutic decisions must be coordinated through your specialist.
Patient Safety Exclusion Criteria & Emergency Red Flags
- Exclusion: Active febrile illness or acute pancreatitis episode โ postpone sample collection until clinically stable.
- Emergency Red Flags: Sudden severe abdominal pain, projectile vomiting, or lethargy in an infant with known hypertriglyceridemia requires immediate emergency care. This test is elective and not for acute presentations.
- Minors: Genetic testing of minors must be ordered by a licensed pediatrician and accompanied by genetic counselling, with consent obtained per Federal Decree-Law No. 4 of 2016 on Medical Liability.
Patient FAQ & Clinical Guidance
1. What does the GPD1 genetic test diagnose?
The GPD1 gene sequencing test detects pathogenic mutations causing transient infantile hypertriglyceridemia (HTGTI), a rare inherited lipid disorder. Identifying the genetic etiology allows precise dietary management to reduce pancreatitis risk and provides reassurance about the typically self-limiting nature of the condition.
2. How is the sample collected and is home service safe?
We offer VIP mobile phlebotomy for blood collection or buccal swab sampling via temperature-controlled cold-chain logistics, ensuring high-quality DNA preservation for accurate NGS results. Our trained phlebotomists use infant-friendly vein-viewing technology and follow UAE infection control protocols, providing a safe and comfortable home experience from 8 AM to 11 PM daily.
3. What is the cost and does insurance cover this test?
The test costs 2,800 AED. We provide direct billing pre-verification via WhatsApp (+971 54 548 8731). Many UAE insurers cover medically necessary genetic testing; we handle all paperwork to ensure no upfront financial surprise.
4. How long does it take to receive results?
The definitive molecular diagnosis requires 3โ4 weeks due to the comprehensive nature of NGS analysis and variant interpretation. Your referring physician will receive a detailed clinical report upon completion.
UAE Regulatory & Data Privacy Adherence
Data Protection: All patient genetic data is processed 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. Your genetic information is encrypted, access-controlled, and never shared without explicit consent.
Clinical Safety & Consent: Sample collection and testing procedures adhere to Federal Decree-Law No. 4 of 2016 on Medical Liability, ensuring patient safety, informed consent, and professional accountability at every step.
Clinical & Logistical Metadata
| Test Name | GPD1 Gene Sequencing for Transient Infantile Hypertriglyceridemia |
| Price (AED) | 2,800 |
| Turnaround Time | 3โ4 weeks |
| Sample Type / Matrix | Peripheral whole blood (3โ5 mL EDTA) or buccal swab โ VIP Mobile Phlebotomy & Temperature-Controlled Cold-Chain Home Collection (available daily 8 AM to 11 PM) |
| Methodology Used | Next-Generation Sequencing (NGS) โ full GPD1 coding region coverage |
| ICD-10-CM Code | E78.1, E78.3 |
| LOINC Code | 55233-1 |
| DHA Facility License & Laboratory Address | DHA License No. 1143 โ Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE | DNA Labs UAE |
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