Test Price
2,800 AED✅ Home Collection Available
NR5A1 Gene (SPGF8) Genetic Test in UAE | 2800 AED | 2026 DHA Guidelines
تحليل جين NR5A1 (فشل تكوين النطاف من النوع 8) بتقنية التسلسل الجيني الشامل من الجيل التالي في الإمارات | 2800 درهم | إرشادات هيئة الصحة بدبي 2026
الموثوقية التشخيصية بنسبة 99.9% عبر معالجة معتمدة بمواصفة الآيزو – نتائج دقيقة في 3 إلى 4 أسابيع
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 Accredited Processing.
- Premium Logistics: Paid Hospital-Grade Home Collection via ISO Certified Cold-Chain Home Collection and VIP Mobile Phlebotomy, covering all Emirates 8 AM–11 PM.
- Clinical Guidance: Telephonic Post-Test Clinical Guidance in result interpretation by a DHA-licensed specialist.
- Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731 – instant pre‑approval for most major UAE networks.
Overview
The NR5A1 Gene (SPGF8) Genetic Test provides a comprehensive analysis of the nuclear receptor subfamily 5 group A member 1 gene, the master regulator of gonadal development and steroidogenesis. This test is crucial for diagnosing spermatogenic failure type 8, 46,XY disorders of sex development, and related reproductive disorders, using high‑coverage next‑generation sequencing for unrivalled detection of single nucleotide variants, small indels, and copy number changes.
يقدم تحليل شامل لجين NR5A1 المسؤول عن تطور الغدد التناسلية، مما يساعد في تشخيص فشل تكوين النطاف من النوع 8 واضطرابات تمايز الجنس 46,XY بدقة عالية.
| Feature | Our NR5A1 NGS Test | Closest Alternative (Sanger Sequencing) |
|---|---|---|
| Diagnostic Precision | 99.9% analytical sensitivity for all coding exons | Limited to single‑amplicon analysis; may miss large deletions |
| Methodology | Next‑Generation Sequencing (NGS) + Sanger confirmation | Sanger sequencing of select exons |
| Turnaround Time | 3–4 weeks | 4–6 weeks (batch‑dependent) |
Physician Insight & Safety Protocol
“Genetic testing of NR5A1 provides a definitive molecular diagnosis for patients with unexplained infertility or ambiguous genitalia; however, results must be interpreted within the full clinical and hormonal context. I strongly recommend a pre‑test genetic counselling session to empower families with realistic expectations. Dr. PRABHAKAR REDDY (DHA: 61713011).”
⚠️ Medication Warning:
Do not discontinue prescribed medication without consulting your doctor. This test does not replace ongoing endocrine or fertility treatment.
Exclusion Criteria & Emergency Red Flags
- Test not performed on minors without both parental/guardian consent and a court‑appointed guardian where required by UAE Child Data Protection laws.
- Patients with active severe infection or haemodynamic instability – address acute condition first.
- Inability to provide an adequate blood or FTA card sample; lipemic or haemolysed samples may be rejected.
- Red Flag: If the individual experiences acute adrenal crisis symptoms (vomiting, severe hypotension, altered consciousness) before or after testing, seek immediate emergency care – this test is not a substitute for urgent medical evaluation.
Patient FAQ & Clinical Guidance
1. What does the NR5A1 gene test detect?
Snippet: This high‑precision NGS assay detects all clinically significant variants in the NR5A1 gene, including point mutations, splice‑site alterations, and exon‑level deletions linked to male infertility and disorders of sex development.
ماذا يكشف تحليل جين NR5A1؟
يكشف التحليل عن الطفرات والحذف في جين NR5A1 المسببة للعقم الذكوري واضطرابات تمايز الجنس بدقة تشخيصية تصل إلى 99.9%.
2. Who should consider this test?
Snippet: Men with non‑obstructive azoospermia, 46,XY disorder of sex development, premature ovarian failure in females, or a family history of NR5A1‑related conditions should consider this comprehensive genetic.
من يجب أن يفكر في إجراء هذا التحليل؟
الرجال المصابون بفقد النطاف غير الانسدادي، أو اضطرابات تمايز الجنس 46,XY، أو السيدات بفشل المبايض المبكر.
3. How is the sample collected and what is the preparation?
Snippet: A simple blood draw or a single drop of blood on an FTA card is collected at our cold‑chain home service after a mandatory genetic counselling session and completion of a detailed family health pedigree.
كيف تُجمع العينة وما هو التحضير المطلوب؟
تُؤخذ عينة دم وريدي أو قطرة دم على بطاقة FTA خلال خدمة منزلية مبرّدة، بعد جلسة إرشاد وراثي وتوثيق التاريخ العائلي.
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All reports reviewed by DHA-Certified physicians