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Test Price

2,800 AED

✅ Home Collection Available

HOXA13 Gene Guttmacher Syndrome Genetic Test in Dubai | 2800 AED | DHA Licensed

Executive Summary & Core Metrics

Why Choose Our Test?

  • Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 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 in result interpretation.
  • Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731.

Test Overview & Methodology

This Next-Generation Sequencing (NGS) test analyses the entire coding region of the HOXA13 gene to identify pathogenic variants associated with Guttmacher syndrome, a rare autosomal dominant disorder characterised by hand-foot-genital anomalies. Our UAE-based, DHA-compliant service delivers clinically actionable results within 3–4 weeks, empowering healthcare providers to guide reproductive and clinical management.

Feature Our Test (Precision/Method/Speed) Closest Alternative
Technology NGS (High-depth, full gene sequencing) Sanger sequencing (single-exon only, limited)
Turnaround Time 3–4 weeks 6–8 weeks
Analytical Sensitivity >99.9% for SNVs, indels ~95% limited to targeted regions

Physician Insight & Safety Protocols

"As a DHA-licensed Consultant Medical Genetics, I recommend this HOXA13 gene test for patients with suspected hand-foot-genital anomalies or a family history of Guttmacher syndrome. A thorough clinical correlation with phenotypic features is essential, as NGS may reveal variants of uncertain significance. Always interpret results in the context of a multidisciplinary team evaluation." — Lina Osama Zaki Quteineh, Consultant Medical Genetics, DHA Registration ID: 9294403

Clinical Advisory

⚠️ Clinical Notice: Do not discontinue prescribed medication without consulting your doctor.

Exclusion Criteria & ER Red Flags

  • Exclusion Criteria: Active coagulopathy, acute infection at venipuncture site, inability to provide informed consent (minors require guardian as per Federal Decree-Law No. 4 of 2016 on Medical Liability).
  • ER Red Flags: Sudden severe bleeding unresponsive to pressure after collection, signs of systemic allergic reaction to antiseptic, or loss of consciousness. Seek immediate medical attention.

Patient FAQ & Clinical Guidance

1. How accurate is the HOXA13 gene NGS test for Guttmacher syndrome diagnosis?

Our NGS platform achieves 99.9% diagnostic sensitivity for single nucleotide variants and small insertion/deletions within the HOXA13 gene, validated against international reference standards.

2. Can I eat or drink before the blood draw for this genetic test?

Yes, fasting is not required; you may eat and drink normally before the blood draw and maintain adequate hydration.

3. Will my insurance cover the HOXA13 gene test in the UAE?

We directly verify coverage with major UAE insurers via WhatsApp at +971 54 548 8731; many plans cover medically necessary genetic testing for reproductive anomalies.

UAE Regulatory & Data Privacy Adherence

Compliance Framework

Our laboratory operates under DHA Facility License No. 1143 and 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. Genetic data is encrypted, access-controlled, and never shared without explicit patient consent. All clinical procedures adhere to Federal Decree-Law No. 4 of 2016 on Medical Liability.

Clinical & Logistical Metadata

Test Name HOXA13 Gene Sequencing (Guttmacher Syndrome)
Price (AED) 2,800
Turnaround Time 3–4 weeks
Sample Type / Matrix Peripheral whole blood (3–5 mL in EDTA tube)
Methodology Used Next-Generation Sequencing (NGS), full coding region + splice sites
ICD-10-CM Code Q87.8
LOINC Code 48007-2
DHA Facility License & Address License No. 1143 | Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE | Corporate Lab: DNA Labs UAE

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