Test Price
2,800 AED✅ Home Collection Available
KIF5C Gene Neurodevelopmental Malformation and Microcephaly Genetic Test in UAE
Executive Summary & Core Metrics
Patient & Clinician Assurance
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 15189‑accredited Next‑Generation Sequencing, validated for KIF5C variant detection.
- Premium Logistics: VIP Mobile Phlebotomy & Temperature‑Controlled Cold‑Chain Home Collection across all Emirates, daily 8 AM – 11 PM.
- Clinical Guidance: Telephonic Post‑Test Clinical Guidance for result interpretation, directly with our medical team.
- Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731.
Test Overview & Methodology
This advanced genetic test sequences the entire coding region of the KIF5C gene using targeted next‑generation sequencing (Illumina® platform) to identify pathogenic variants causative of neurodevelopmental malformations and microcephaly. It provides a definitive molecular diagnosis for affected children and adults, guiding personalized management and family planning with UAE regulatory precision.
| Feature | Our KIF5C NGS Test | Closest Alternative (Whole Exome Sequencing) |
|---|---|---|
| Diagnostic Precision | >99.9% for KIF5C variants | ~95% coverage, may miss deep intronic changes |
| Methodology | Targeted NGS (Illumina® platform) | Whole Exome Capture + Sequencing |
| Turnaround Time | 2–3 Weeks | 4–6 Weeks |
| Price (AED) | 2800 | 4500–5500 |
Physician Insight & Safety Protocols
“As a consultant medical geneticist, I emphasize that a positive KIF5C variant provides a definitive aetiology for microcephaly and neurodevelopmental delay, enabling targeted family counselling and surveillance. However, a negative result does not exclude other genetic causes; comprehensive evaluation with chromosomal microarray and brain imaging remains essential.”
— Lina Osama Zaki Quteineh, Consultant Medical Genetics, DHA Registration ID: 9294403
Medication Advisory
Do not discontinue or adjust any prescribed medication without direct consultation with your treating physician. Results of this genetic test are for diagnostic and prognostic purposes only and do not imply immediate changes to management unless advised by a healthcare professional.
Safety Exclusion Criteria & Red Flags
- Exclusion: Patients without clinical microcephaly or neurodevelopmental delay; samples not meeting collection standards; children without documented guardian consent as per Federal Decree‑Law No. 4 of 2016 on Medical Liability.
- Emergency Red Flags: Acute onset seizures, unexplained loss of consciousness, sudden neurological deterioration, severe headache with vomiting – seek immediate emergency medical care.
Patient FAQ & Clinical Guidance
1. What does the KIF5C gene test detect and how is it performed?
This test detects pathogenic KIF5C variants causing neurodevelopmental malformations and microcephaly via next-generation sequencing of blood DNA. Only a 3 mL EDTA blood sample, one drop on an FTA card, or previously extracted DNA is required. The sample is processed in our ISO‑accredited facility using a targeted capture panel and bioinformatics pipeline aligned to international diagnostic standards. Results are reported with ACMG variant classification and clinical correlation guidance.
2. Who should consider this test and when is it recommended?
Physicians should order this test for patients presenting with congenital microcephaly, global developmental delay, or brain malformations with no clear alternative diagnosis. It is particularly recommended for children under evaluation by a paediatric neurologist, those with a family history suggestive of autosomal dominant KIF5C‑related disorders, and individuals pursuing preconception genetic counselling. A clinical geneticist consultation is mandatory prior to testing in the UAE.
3. How long do results take and what happens after I receive them?
Final results are delivered within two to three weeks, and you receive a telephonic clinical guidance session to interpret findings. The report details any detected variant, its ACMG classification, and its potential impact on health. A qualified DHA‑licensed clinical geneticist or neurologist will explain the clinical relevance and may recommend additional family screening or imaging. All data is handled in strict compliance with UAE PDPL, and only the ordering physician and patient receive the report.
UAE Regulatory & Data Privacy Adherence
Legal & Quality Compliance
This test is performed under the mandates of Federal Decree‑Law No. 4 of 2016 on Medical Liability ensuring clinical accountability, Federal Decree‑Law No. 45 of 2021 on Personal Data Protection (PDPL) for secure handling of genetic information, and Federal Law No. 2 of 2019 Concerning the Use of Information and Communication Technology in Health Fields for health data governance.
Our facility holds ISO 9001:2015 Certification (INT/EGQ/2509DA/3139) and operates under DHA & MOHAP guidelines. Genetic results are for diagnostic purposes only; do not self‑prescribe or alter medications based on this information without medical advice.
📞 WhatsApp Support & Bookings: +971 54 548 8731 | Home Collection Hotline 8:00 AM – 11:00 PM
Clinical & Logistical Metadata
| Test Name | KIF5C Gene Neurodevelopmental Malformation and Microcephaly Genetic Test |
| Price (AED) | 2,800 |
| Turnaround Time | 2–3 Weeks |
| Sample Type / Matrix | Whole Blood (EDTA) or FTA card (3 mL) |
| Methodology Used | Targeted Next‑Generation Sequencing (Illumina® platform) |
| ICD-10-CM Code | Q02 (Microcephaly), Q04.8 (Other specified congenital malformations of brain) |
| LOINC Code | 101339-6 (KIF5C gene mutation analysis) |
| DHA Facility License & Laboratory Address | DHA License No. 1143 – Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE. Corporate Lab: DNA Labs UAE |
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Available in Arabic, English, Hindi & Urdu
ISMS 27001:2022
ISO Accredited
HIPAA
All reports reviewed by DHA-Certified physicians