Also known as: B9D1 Gene NGS Test, Meckel Syndrome Type 9 Genetic Panel
Test Price
2,800 AEDโ Home Collection Available
๐ Results in 3โ4 Weeks
B9D1 Gene Meckel Syndrome Type 9 Genetic Test in UAE | 2800 AED
Executive Summary & Core Metrics
Clinical & Operational Assurance
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 Accredited Processing (Cert: INT/EGQ/2509DA/3139).
- Premium Logistics: VIP Mobile Phlebotomy & Temperature-Controlled Cold-Chain Home Collection (Available daily 8 AM โ 11 PM).
- Clinical Guidance: Telephonic Post-Test Clinical Guidance in result interpretation by DHA-licensed specialists.
- Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731.
Test Overview & Methodology
The B9D1 Gene Meckel Syndrome Type 9 NGS Test is a high-precision next-generation sequencing assay that scrutinizes the entire coding region of the B9D1 gene to confirm or exclude Meckel syndrome type 9. This disorder is a severe autosomal recessive ciliopathy affecting the liver, kidneys, and endocrine system, making early molecular diagnosis critical for clinical management and family planning.
| Parameter | Our Test (Premium Diagnostics UAE) | Closest Alternative (Routine NGS Panel) |
|---|---|---|
| Precision | Single-gene high-depth NGS with full exon coverage of B9D1 | May be embedded in larger panel with reduced coverage depth |
| Methodology | NGS with Sanger confirmation of all pathogenic variants | NGS only; confirmatory step often omitted |
| Turnaround | 3โ4 Weeks with expedited WhatsApp updates | 4โ6 Weeks; no dedicated client portal |
| Pre-Test Genetic Counselling | Mandatory complimentary session by DHA-licensed counselor | Optional or self-referred without integrated support |
Physician Insight & Safety Protocols
Lina Osama Zaki Quteineh | Consultant Medical Genetics | DHA Registration ID: 9294403: โA positive B9D1 variant alone does not predict the full phenotypic spectrum; clinical correlation with hepatic, renal, and endocrine imaging is essential. I strongly advise that this test be used in conjunction with a multidisciplinary consultation, especially when planning future pregnancies. Your doctor remains the cornerstone of safe interpretation.โ
Advisory: Medication and Test Interaction
Do not discontinue prescribed medication without consulting your doctor. This genetic test is intended for diagnostic clarification and does not replace ongoing clinical treatment or monitoring.
Exclusion Criteria & Emergency Red Flags
- Exclusion Criteria: Inability to provide informed consent (legal guardian required for minors); active febrile illness that may interfere with DNA stability (postpone venipuncture); known hematological disorders that contraindicate blood draw.
- ER Red Flags: If you experience severe abdominal distension, intractable vomiting, jaundice, or sudden neurological changes while awaiting results, immediately visit the nearest hospital emergency department. Do not wait for genetic test results.
Patient FAQ & Clinical Guidance
1. Why is the B9D1 gene test necessary if an ultrasound already detected kidney cysts?
A: Ultrasound findings alone cannot distinguish Meckel syndrome type 9 from other ciliopathies. Definitive molecular diagnosis guides targeted clinical management and family risk assessment.
2. Can I use a home-collected sample for this test, and how is the chain of custody maintained?
A: Yes, our DHA-licensed mobile phlebotomists collect blood or saliva samples under strict ISO cold-chain protocols with tamper-evident labeling from your doorstep to our lab.
3. What happens if a variant of uncertain significance (VUS) is reported?
A: Our clinical team will provide a complimentary 15-minute telehealth session to explain the VUS, recommend family segregation studies, and update you if reclassification occurs within two years.
UAE Regulatory & Data Privacy Adherence
Regulatory Compliance Framework
All patient 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. Clinical testing safety and patient consent adhere to Federal Decree-Law No. 4 of 2016 on Medical Liability. This genetic test is regulated under UAE genetic testing guidelines; for insurance verification or to schedule a home draw, WhatsApp +971 54 548 8731.
Clinical & Logistical Metadata
| Test Name | B9D1 Gene Meckel Syndrome Type 9 Genetic Test (NGS) |
| Price (AED) | 2,800 |
| Turnaround Time | 3โ4 Weeks |
| Sample Type / Matrix | Peripheral Whole Blood (EDTA) or Saliva (Oragene DNA Kit) |
| Methodology Used | Next-Generation Sequencing (NGS) with Sanger confirmation |
| ICD-10-CM Code | Q61.8 |
| LOINC Code | 56367-6 |
| DHA Facility License & Laboratory Address | DHA Facility License Number: 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
Preparation Required
["No fasting required", "Do not discontinue prescribed medication"]
Medically Reviewed by Dr. Lina Osama Zaki Quteineh
All content reviewed by qualified professionals for accuracy.
ISMS 27001:2022
ISO Accredited
HIPAA
All reports reviewed by DHA-Certified physicians