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Test Price

2,800 AED

✅ Home Collection Available

GRID2 Gene Spinocerebellar Ataxia Type 18 (Autosomal Recessive) Genetic Test in UAE | 2,800 AED | DHA Licensed

Executive Summary & Core Metrics

Core Metrics

  • 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 from 8 AM to 11 PM).
  • Clinical Guidance: Telephonic Post-Test Clinical Guidance in result interpretation with a DHA‑licensed Consultant Medical Genetics.
  • Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731.

Test Overview & Methodology

The GRID2 Gene Spinocerebellar Ataxia Type 18 NGS Test detects pathogenic variants in the GRID2 gene with unrivaled depth and accuracy, enabling definitive molecular diagnosis of this autosomal recessive neurodegenerative disorder.

Feature Our GRID2 NGS Test Closest Alternative (Single‑Gene Sanger Sequencing)
Methodology Next‑Generation Sequencing (NGS) with full gene coverage and CNV analysis Sanger sequencing of selected exons only
Diagnostic Yield >98% for GRID2 variants, including deep intronic and structural variants ~80%, limited to known common mutations
Turnaround Time 3–4 Weeks 4–6 Weeks
Pre‑Test Requirement Includes mandatory genetic counselling session and pedigree charting Often omitted; counselling not integrated

Physician Insight & Safety Protocols

“As a Consultant Medical Genetics, I recognize that a genetic test result is only one piece of the diagnostic puzzle. I strongly advise that every patient discuss their GRID2 NGS result with their treating neurologist and a certified genetic counsellor. Clinical correlation, family history, and neurological examination are essential before any medical decision is made. Never discontinue prescribed medications without consulting your doctor.” — Lina Osama Zaki Quteineh, Consultant Medical Genetics, DHA Registration ID: 9294403

Medication Safety Advisory

Important Notice

Do not discontinue prescribed medication without consulting your doctor. Abrupt cessation of anti‑epileptics, muscle relaxants, or any neurological drug may provoke severe withdrawal symptoms, seizure relapse, or status epilepticus.

Safety Exclusion Criteria & Emergency Red Flags

  • Exclusion criteria for home collection: Active febrile illness, ongoing acute neurological decompensation, inability to provide informed consent, or patient under 18 years without a legal guardian as mandated by Federal Law No. 2 of 2019 concerning the Use of ICT in Health Fields.
  • Pregnancy: Testing is generally not recommended unless clinically justified after genetic counselling, as results may have implications for reproductive planning.
  • Emergency Red Flags – Seek immediate medical attention (call 998 or visit ER) if you experience: sudden, severe worsening of gait instability, frequent falls, swallowing difficulties with choking, or sudden onset of respiratory distress.
  • Prior to specimen collection, a comprehensive clinical history and formal genetic counselling session to construct a detailed pedigree chart are mandatory.

Patient FAQ & Clinical Guidance

1. What is the GRID2 spinocerebellar ataxia type 18 NGS test, and who should consider it?

This NGS-based genetic test provides definitive molecular confirmation of biallelic GRID2 mutations, helping neurologists and geneticists confirm autosomal recessive spinocerebellar ataxia type 18 in patients with progressive cerebellar ataxia and a relevant family history.

2. How is the test performed and what sample is needed?

A simple blood sample, extracted DNA, or a single drop of blood on an FTA card is collected by a certified phlebotomist during an 8 AM – 11 PM home visit, then transported under strict cold‑chain conditions for NGS analysis.

3. What do the results mean and will I receive clinical support?

A positive result identifies disease‑causing GRID2 variants, enabling precise carrier testing for family members and prenatal options; a negative result, however, does not exclude other hereditary ataxias, requiring further neurological evaluation.

For post‑clinical guidance, WhatsApp +971 54 548 8731 to schedule a tele‑consultation.

UAE Regulatory & Data Privacy Adherence

DNA Labs UAE strictly adheres to the 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 and patient consent protocols comply with Federal Decree-Law No. 4 of 2016 on Medical Liability. This test is processed under ISO 9001:2015 quality management (Cert: INT/EGQ/2509DA/3139).

Clinical & Logistical Metadata

Test Name GRID2 Gene Spinocerebellar Ataxia Type 18 (Autosomal Recessive) NGS Genetic Test
Price (AED) 2,800
Turnaround Time 3–4 Weeks
Sample Type / Matrix Peripheral Whole Blood, Extracted DNA, or FTA Card Specimen
Methodology Used Next-Generation Sequencing (NGS) with full gene coverage and CNV analysis
ICD-10-CM Code G11.8 (Other hereditary ataxias)
LOINC Code 81247-9 (Neurology Genetic Disease Sequencing Panel)
DHA Facility License & Laboratory Address DHA License No: 1143 | Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE | DNA Labs UAE

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