Test Price
2,800 AED✅ Home Collection Available
MED12 Gene FG Syndrome Type 1 Genetic Testing (NGS) in UAE | 2800 AED
Executive Summary & Core Metrics
Executive Summary: This ISO 9001:2015‑certified diagnostic test delivers 99.9% diagnostic sensitivity for MED12‑related FG syndrome type 1 through high‑depth Next‑Generation Sequencing. The service includes VIP mobile phlebotomy with temperature‑controlled cold‑chain home collection, post‑test tele‑clinical guidance by a DHA‑licensed geneticist, and direct insurance verification via WhatsApp at +971 54 548 8731.
Core Metrics: Analytical sensitivity >99.9%; turnaround time 3–4 weeks; sample types accepted include peripheral whole blood (EDTA), extracted DNA, or FTA card; price 2,800 AED inclusive of genetic counselling.
Test Overview & Methodology
The MED12 gene test employs Next‑Generation Sequencing (NGS) to detect pathogenic variants responsible for FG syndrome type 1, an X‑linked condition characterized by intellectual disability, hypotonia, and distinctive facial features. All coding regions and splice sites are covered at high depth; any detected variants are confirmed via Sanger sequencing. A pre‑test genetic counselling session is mandatory to document family pedigree and obtain informed consent.
Turnaround time is 3–4 weeks from sample receipt at our ISO‑accredited laboratory. Home collection is available daily from 8 AM to 11 PM.
| Parameter | Our MED12 NGS Test | Closest Alternative (Whole Exome Sequencing) |
|---|---|---|
| Precision | >99.9% analytical sensitivity for MED12 coding & splice regions | ~95% sensitivity for MED12 due to lower depth; may miss deep intronic variants |
| Method | Focused NGS with 100% MED12 gene coverage, validated Sanger confirmation | Broad exome with variable coverage; incidental findings possible |
| Turnaround Time | 3–4 weeks | 6–8 weeks |
Physician Insight & Safety Protocols
Lina Osama Zaki Quteineh | Consultant Medical Genetics | DHA Registration ID: 9294403
“A definitive diagnosis of FG syndrome type 1 requires careful clinical correlation with the genetic result. A positive MED12 variant confirms the diagnosis, but a negative result does not exclude other genetic or acquired neurological disorders. Interpretation must integrate the child’s developmental profile, imaging findings, and family history. Genetic counselling is essential for all families.”
Clinical Advisory
Medication Warning: Do not discontinue any prescribed medication without consulting your attending physician. Abrupt cessation may lead to serious clinical deterioration, especially in patients on neurodevelopmental therapies.
Exclusion Criteria & Emergency Red Flags
- Exclusion for home collection: Severe needle phobia or known bleeding diathesis – please inform the phlebotomist so that a hospital-based draw can be arranged.
- Emergency warning: If the patient experiences new‑onset seizures, loss of consciousness, or acute neurological decline, seek immediate hospital emergency care; do not wait for scheduled phlebotomy.
- Neonatal/pediatric: In infants, urgent metabolic or structural brain abnormalities must be ruled out by a paediatric neurologist before genetic sampling.
Patient FAQ & Clinical Guidance
1. What is the MED12 Gene FG Syndrome Type 1 Test?
This test analyses the MED12 gene via Next‑Generation Sequencing to diagnose FG syndrome type 1, an X‑linked intellectual disability syndrome with multi‑system involvement including hypotonia, distinctive facial features, and developmental delay.
2. How is the sample collected and what is the turnaround time?
A blood sample (peripheral whole blood EDTA), extracted DNA, or FTA card is collected by a certified phlebotomist during a home visit. VIP mobile phlebotomy with cold‑chain logistics is available daily from 8 AM to 11 PM. Results are delivered in 3–4 weeks.
3. Is genetic counselling required before testing?
Yes, a pre‑test genetic counselling session is mandatory to draw the family pedigree, assess carrier risk, discuss implications of results, and secure informed consent. Our genetic counsellor will coordinate this before sample collection.
4. Will the test detect all types of FG syndrome?
This targeted NGS test specifically covers MED12 coding and splice regions. It diagnoses only FG syndrome type 1. Other types of FG syndrome caused by different genes (e.g., MED12L, FMR1) are not detected. Whole exome or genome sequencing may be considered if clinical suspicion remains high after a negative result.
UAE Regulatory & Data Privacy Adherence
This service fully complies 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 safety and patient consent are governed by Federal Decree-Law No. 4 of 2016 on Medical Liability. All genetic data is encrypted and stored in secure UAE data centers. The laboratory is accredited to ISO 9001:2015 (Cert: INT/EGQ/2509DA/3139) and licensed by the Dubai Health Authority under facility license number 1143.
Clinical & Logistical Metadata
| Test Name | MED12 Gene FG Syndrome Type 1 Genetic Testing (NGS) |
| Price (AED) | 2,800 AED |
| Turnaround Time | 3–4 weeks |
| Sample Type / Matrix | Peripheral whole blood (EDTA), extracted DNA, or FTA card. VIP Mobile Phlebotomy & Temperature‑Controlled Cold‑Chain Home Collection available daily 8 AM–11 PM. |
| Methodology Used | Next‑Generation Sequencing (NGS) with Sanger confirmation |
| ICD-10-CM Code | Q87.8 (Other specified congenital malformation syndromes affecting multiple systems) |
| LOINC Code | 87422-4 |
| DHA Facility License & Laboratory Address | DHA License: 1143 | Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE | DNA Labs UAE |
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