Test Price
2,800 AED✅ Home Collection Available
XRCC4 Gene Genetic Test (Short Stature, Microcephaly, Endocrine Dysfunction) in UAE | 2800 AED | 2026 DHA Guidelines
تحليل جين XRCC4 في الإمارات | 2800 درهم | معتمد من هيئة الصحة بدبي
الملخص التنفيذي
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 Certified Processing (Cert: INT/EGQ/2509DA/3139).
- Premium Logistics: Paid Hospital-Grade Home Collection via ISO Certified Cold-Chain Home Collection and VIP Mobile Phlebotomy.
- Clinical Guidance: Telephonic Post-Test Clinical Guidance in result interpretation.
- Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731.
Overview
XRCC4 gene DNA sequencing via Next-Generation Sequencing (NGS) identifies mutations responsible for short stature, microcephaly, and endocrine dysfunction, enabling precise diagnosis and genetic counseling. This non-invasive test requires only a blood sample or DNA and delivers results within 3–4 weeks.
للملخص: يكشف تحليل تسلسل جين XRCC4 بتقنية الجيل التالي عن الطفرات المرتبطة بقصر القامة وصغر الرأس والخلل الهرموني، مما يساعد في التشخيص الدقيق والإرشاد الوراثي.
| Feature | Our Test | Closest Alternative |
|---|---|---|
| Precision | Full gene NGS coverage with variant confirmation | Limited targeted mutation panel |
| Methodology | Next-Generation Sequencing (NGS) | Sanger sequencing (single gene) |
| Turnaround Time | 3–4 Weeks | 6–8 Weeks |
Physician Insight & Safety Protocol
Dr. PRABHAKAR REDDY (DHA License: 61713011) notes: "While a positive result in the XRCC4 gene strongly correlates with the clinical triad of growth failure, microcephaly, and hormonal disturbance, it must always be interpreted alongside the patient's full clinical picture. This test provides crucial prognostic and management insights, especially for initiating early endocrine interventions and cancer surveillance. I urge patients and families to discuss findings thoroughly with their genetic counselor and pediatric endocrinologist."
Medication Warning:
Do not discontinue prescribed medication without consulting your doctor.
Exclusion Criteria: Inability to provide informed consent (legal guardian required for minors under CDS Law 2026), active severe illness precluding safe blood draw, known alternative diagnosis not warranting genetic testing.
ER Red Flags: If patient develops severe growth arrest, unexplained recurrent infections, or neurological deterioration, seek immediate medical evaluation regardless of test pending status.
Patient FAQ & Clinical Guidance
What is the XRCC4 gene test and who should consider it?
This test sequences the entire XRCC4 gene to detect mutations causing short stature, microcephaly, and endocrine dysfunction. It is recommended for children with unexplained growth failure, microcephaly, and hormonal abnormalities, and for families seeking a definitive genetic diagnosis.
كيف يتم إجراء تحليل جين XRCC4 وما هي مدة النتيجة؟
يتم سحب عينة دم بسيطة من المنزل بواسطة فريق تمريض متنقل، ثم يُحلل الحمض النووي بتقنية الجيل التالي وتظهر النتيجة خلال 3 إلى 4 أسابيع.
How accurate is the test and how should I prepare?
With 99.9% diagnostic sensitivity under ISO 9001:2015 protocols, it provides highly reliable mutation detection. Preparation includes a mandatory pre- genetic counseling session to document family history (pedigree) and obtain informed consent, as per DHA guidelines.
UAE Regulatory Compliance: This service adheres to Federal Decree-Law No. 41 of 2024 (Art. 87) on genetic testing, UAE Personal Data Protection Law (PDPL) for data privacy, and the 2026 CDS Law safeguarding minors. Accredited by ISO 9001:2015 (Cert: INT/EGQ/2509DA/3139).
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All reports reviewed by DHA-Certified physicians