Test Price
2,800 AEDโ Home Collection Available
SDHD Gene Pheochromocytoma Type 1 Genetic Test in UAE | AED 2800 | DHA Licensed Laboratory
Executive Summary & Core Metrics
The SDHD Gene Pheochromocytoma Type 1 Genetic Test employs next-generation sequencing (NGS) for high-sensitivity detection of pathogenic variants in the SDHD tumor suppressor gene. This ISO 9001:2015 accredited assay achieves >99.9% diagnostic sensitivity for single-nucleotide variants, indels, and copy number changes across all coding exons and flanking intronic regions.
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO Accredited Processing.
- Premium Logistics: VIP Mobile Phlebotomy & Temperature-Controlled Cold-Chain Home Collection (daily 8 AM โ 11 PM).
- Clinical Guidance: Telephonic Post-Test Clinical Guidance in result interpretation.
- Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731.
Test Overview & Methodology
The SDHD Gene Pheochromocytoma Type 1 Genetic Test uses next-generation sequencing to detect pathogenic variants across all coding exons and flanking intronic regions of the SDHD tumor suppressor gene. This gold-standard test enables definitive diagnosis, risk stratification, and surveillance planning for individuals with a personal or family history of neuroendocrine tumors. The methodology includes full gene sequencing with copy number analysis, ensuring detection of large deletions/duplications missed by traditional Sanger sequencing.
| Feature | Our Test (NGS Sequencing) | Closest Alternative (Single-Gene Sanger) |
|---|---|---|
| Coverage | Full SDHD gene (exons + 20 bp intronic boundaries) | Limited to predefined hotspot mutations |
| Sensitivity | >99.9% for single-nucleotide variants, indels, and copy number changes | ~85% (misses large deletions/duplications) |
| Turnaround Time | 3โ4 Weeks | 6โ8 Weeks |
| Home Collection | Yes (Cold-chain, VIP Phlebotomy) | Not offered |
| ISO 9001:2015 Accreditation | Yes (Cert: INT/EGQ/2509DA/3139) | Unverified |
Physician Insight & Safety Protocols
โAs a Consultant Medical Genetics, I advise that this SDHD test is a powerful tool for confirming hereditary pheochromocytoma-paraganglioma syndrome. Results must be interpreted alongside biochemical markers, imaging findings, and a detailed family pedigree. A positive result does not mean active diseaseโit signifies elevated lifelong risk requiring specialist surveillance.โ โ Lina Osama Zaki Quteineh (DHA Registration ID: 9294403), Consultant Medical Genetics
Advisory: Medication & Clinical Precaution
Do not discontinue prescribed medication without consulting your doctor. Abruptly stopping antihypertensives or tumor-related treatments can trigger life-threatening cardiovascular events. Always inform your physician of all medications and supplements before genetic testing.
Exclusion Criteria & Emergency Red Flags
- Absolute Exclusion: Patients in acute hypertensive crisis (BP > 180/120 mmHg) until stabilized in a hospital setting.
- Relative Exclusion: Active febrile illness or recent blood transfusion (< 2 weeks) โ may delay collection.
- Pediatric Consideration: Individuals under 18 years require informed consent from legal guardian per Federal Decree-Law No. 4 of 2016 on Medical Liability.
- Emergency Red Flags: Sudden severe headache, palpitations, profuse sweating, chest pain, or loss of consciousness โ seek immediate emergency room evaluation (call 998 in UAE). Do not wait for genetic test results.
Patient FAQ & Clinical Guidance
1. What does a positive SDHD test mean for my health and my family?
A positive result confirms a hereditary mutation in the SDHD gene that significantly increases lifetime risk of developing pheochromocytomas and paragangliomas, warranting annual biochemical screening and imaging surveillance. First-degree relatives should consider predictive testing and genetic counseling.
2. How is sample collection performed, and can it be done at home?
A simple venous blood draw (EDTA tube) is all that is required; our ISO-certified phlebotomist visits your home between 8 AM and 11 PM, ensuring cold-chain integrity. The sample is transported to our ISO 9001:2015 accredited laboratory for processing.
3. How are private genetic data protected under UAE law?
All genetic information is encrypted and stored in 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. Results are disclosed only to the ordering physician and the tested individual.
4. What is the turnaround time for results?
The standard turnaround time is 3โ4 weeks from sample receipt. You will receive a comprehensive report including variant classification, clinical interpretation, and recommendations for surveillance.
UAE Regulatory & Data Privacy Adherence
Data Privacy & Compliance Framework
- Personal Data Protection: Fully compliant with Federal Decree-Law No. 45 of 2021 (PDPL), ensuring encryption, access control, and data minimization.
- Health Information Technology: Adheres to Federal Law No. 2 of 2019 for secure electronic health data exchange.
- Medical Liability & Consent: Genetic testing for minors requires guardian consent under Federal Decree-Law No. 4 of 2016 on Medical Liability.
- Accreditation: DNA Labs UAE holds ISO 9001:2015 certification (Cert: INT/EGQ/2509DA/3139) and operates under DHA Facility License 1143.
Clinical & Logistical Metadata
| Test Name | SDHD Gene Pheochromocytoma Type 1 Genetic Test (NGS) |
| Price (AED) | 2,800 |
| Turnaround Time | 3โ4 Weeks |
| Sample Type / Matrix | Peripheral Whole Blood (EDTA) or Extracted DNA |
| Methodology Used | Next-Generation Sequencing (NGS) โ Full gene sequencing with copy number analysis |
| ICD-10-CM Code | D35.0 (Benign neoplasm of adrenal gland) / Z13.8 (Encounter for screening for other specified disease) |
| LOINC Code | 21763-6 (SDHD gene mutation analysis) |
| DHA Facility License & Laboratory Address | License No: 1143 | Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE โ DNA Labs UAE |
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Available in Arabic, English, Hindi & Urdu
ISMS 27001:2022
ISO Accredited
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All reports reviewed by DHA-Certified physicians