Test Price
2,800 AED✅ Home Collection Available
SOHLH1 Gene Oogenesis Dysfunction Genetic Test in UAE | 2800 AED | 2026 DHA Guidelines
تحليل جين SOHLH1 لضعف تكوين البويضات في الإمارات | 2800 درهم | معتمد من هيئة الصحة بدبي
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 accredited processing (Cert: INT/EGQ/2509DA/3139).
- Premium Logistics: Paid hospital-grade home collection via ISO-certified cold-chain logistics and VIP mobile phlebotomy.
- Clinical Guidance: Complimentary telephonic post-test guidance with a genetic specialist to interpret your results.
- Insurance: Direct billing verification via WhatsApp at +971 54 548 8731.
يضمن هذا التحليل دقة تشخيصية بنسبة 99.9% عبر معالجة معتمدة وفقًا لمواصفة ISO، ويشمل خدمة جمع العينات المنزلية المبردة بجودة طبية عالية.
Clinical Overview
The SOHLH1 gene oogenesis dysfunction test uses Genetic Test provides both clinical and research insights for couples planning assisted reproduction.
| Feature | Our NGS Test | Sanger Sequencing Alternative |
|---|---|---|
| Analytical Method | Full coding region NGS (99.9% sensitivity) | Targeted single‑exon analysis (lower sensitivity) |
| Turnaround Time | 3–4 Weeks | 1–2 Weeks (limited coverage) |
| Variant Coverage | All known pathogenic and novel variants | Pre‑defined hotspot mutations only |
Physician Insight & Safety Protocol
"As your physician, I emphasize that genetic results must be interpreted in the context of your complete clinical history; this test does not replace a thorough reproductive evaluation. Always continue prescribed treatments unless otherwise advised. Immediate medical attention is required if you experience severe pelvic pain or signs of ovarian hyperstimulation."
— Dr. PRABHAKAR REDDY, DHA License: 61713011
⚠️ Medication Warning: Do not discontinue any prescribed medication without consulting your doctor. Genetic test results are for clinical correlation only.
Patient Safety & Exclusion Criteria
- Not suitable if you are currently on anticoagulant therapy without prior medical clearance.
- Exclusion if active infection or dermatitis at the venipuncture site is present.
- Emergency Red Flags: Seek urgent medical care if you experience sudden abdominal pain, severe swelling, or signs of a systemic allergic reaction after sample collection.
Patient FAQ & Clinical Guidance
1. What is the role of the SOHLH1 gene in female fertility?
SOHLH1 gene mutations impair oocyte development, causing primary ovarian insufficiency and infertility in women diagnosed via NGS.
طفرات جين SOHLH1 تضعف نمو البويضات، مما يسبب قصور المبيض الأولي والعقم لدى النساء، ويتم تشخيصها عبر التسلسل الجيني.
2. How accurate is this genetic test for oogenesis dysfunction?
With 99.9% diagnostic sensitivity, it identifies all known disease‑causing SOHLH1 variants accurately using advanced NGS technology.
بدقة تشخيصية تصل إلى 99.9%، يحدد هذا الاختبار جميع الطفرات المرضية المعروفة في جين SOHLH1 باستخدام تقنية التسلسل الجيني المتقدم.
3. Do I need genetic counselling before the SOHLH1 test?
Yes, a pre‑ genetic counselling session is mandatory to explain results and pedigree analysis for UAE patients.
نعم، جلسة الاستشارة الوراثية قبل الاختبار ضرورية لشرح النتائج وتحليل شجرة العائلة للمرضى في الإمارات.
دعم ثنائي اللغة متاح
التحقق من التغطية التأمينية
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Stop the guesswork. Send a photo of your Insurance Card and Doctor's Prescription to our DHA-Certified Verification Team on WhatsApp.
توقف عن التخمين. أرسل صورة من بطاقة التأمين ووصفة الطبيب إلى فريق التحقق المعتمد من هيئة الصحة بدبي عبر الواتساب. احصل على تحديث الحالة في دقائق.
Available in Arabic, English, Hindi & Urdu
ISMS 27001:2022
ISO Accredited
HIPAA
All reports reviewed by DHA-Certified physicians