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Test Price

2,800 AED

✅ Home Collection Available

AIFM1 Gene Deafness, X-Linked Type 5 Genetic Test in UAE

Executive Summary & Core Metrics

✓ Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 15189 & ISO 9001:2015 Accredited Processing

✓ 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 for Result Interpretation by DHA-Licensed Genetic Counsellors

✓ Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731

Test Overview & Methodology

The AIFM1 NGS test provides a comprehensive genetic analysis of the AIFM1 gene to diagnose X‑linked deafness type 5 (DFNX5), auditory neuropathy spectrum disorder, and related neurological phenotypes. It uses next‑generation sequencing to detect single nucleotide variants, insertions/deletions, and copy number variations across the entire gene.

FeatureOur Test (AIFM1 NGS)Closest Alternative (Single‑Gene Sanger)
PrecisionFull gene coverage, deep intronic & copy number variantsOnly targeted known mutations; misses novel/structural variants
MethodNext Generation Sequencing (Illumina®) with CNV analysisCapillary sequencing of selected exons
Turnaround3–4 Weeks (definitive)2–3 Weeks (often requires reflex test)

Physician Insight & Safety Protocols

“As a Consultant Medical Genetics, I remind all patients that genetic test results must be interpreted in the context of audiological, neurological, and family history. A negative result does not rule out other causes, and any therapeutic decision must be made jointly with your clinician.” – Lina Osama Zaki Quteineh, DHA License 9294403

Medication & Clinical Caution

Do not discontinue prescribed medication or hearing aids without consulting your doctor. This test is for diagnostic clarification only and does not replace ongoing audiological care.

Exclusion Criteria & Emergency Red Flags

  • Active febrile illness or systemic infection – reschedule home collection.
  • Severe anaemia (Hb < 7 g/dL) may affect phlebotomy safety – contact our team.
  • Results are not actionable in isolation; sudden hearing loss, acute vertigo, or focal neurological deficits demand immediate emergency room evaluation.

Patient FAQ & Clinical Guidance

1. What is the AIFM1 genetic test, and who should consider it?

Snippet: This NGS test detects mutations in the AIFM1 gene causing X‑linked deafness and auditory neuropathy, recommended for males with early‑onset hearing loss and families with a history of X‑linked inheritance.

2. How is the test performed, and what preparation is required?

Snippet: A single blood sample is collected by a phlebotomist at your home; no fasting is needed, just provide a detailed family pedigree and recent audiology reports before collection.

3. What do my results mean for my family and my hearing management?

Snippet: A pathogenic AIFM1 variant confirms X‑linked deafness, guiding family counselling, early cochlear implantation candidacy, and identifying carrier females for reproductive planning within your family.

UAE Regulatory & Data Privacy Adherence

This test is performed 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. The laboratory is fully licensed by the Dubai Health Authority (DHA) under facility number 1143. All genetic data is handled with strict confidentiality and stored in accordance with national health information security standards.

Clinical & Logistical Metadata

Test Name AIFM1 Gene Deafness, X-Linked Type 5 Genetic Test
Price (AED) 2,800
Turnaround Time 3–4 Weeks
Sample Type / Matrix Peripheral whole blood (EDTA)
Methodology Used Next Generation Sequencing (Illumina®) with CNV analysis
ICD-10-CM Code H90.3
LOINC Code 81294-9
DHA Facility License & Laboratory Address License #1143 | Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE

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