Test Price
850 AED✅ Home Collection Available
Female Hypogonadism Panel in UAE | 850 AED | DHA Licensed Lab
Executive Summary & Core Metrics
Executive Summary
Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 Accredited Processing (Cert: INT/EGQ/2509DA/3139).
Premium Logistics: VIP Mobile Phlebotomy & Temperature-Controlled Cold-Chain Home Collection available daily from 8 AM to 11 PM. Samples processed within 2 hours of draw.
Clinical Guidance: Telephonic Post-Test Clinical Guidance with a senior endocrinologist to explain results in full context.
Insurance: Direct Billing Verification via WhatsApp at +971 54 548 8731.
Test Overview & Methodology
This advanced panel precisely measures key ovarian and pituitary hormones including FSH, LH, estradiol, AMH, prolactin, and TSH to classify primary versus secondary hypogonadism. Preferred sampling time is Day 2 or Day 3 of the menstrual cycle, collected in the morning. Sample: 2 mL serum from a Red Top (No Additive) tube; shipped refrigerated or frozen.
| Feature | Our Test – Female Hypogonadism Panel | Standard Hospital-Based Panel |
|---|---|---|
| Methodology | CLIA (broad screening) + LC-MS/MS (gold-standard precision for low-level hormones) | CLIA only; LC-MS/MS rarely available for routine panels |
| Turnaround Time | 3 working days (sample collected Mon/Thu by 9 am; report Wed/Sat) | 5-7 days average |
| Preanalytical Control | ISO-certified cold chain home collection; samples processed within 2 hours of draw | Variable; outpatient collection stability may not be guaranteed |
| Physician Review | Interpretation guidance included, optional tele-consult with an endocrinologist | Report generation only; specialist review out of pocket |
Physician Insight & Safety Protocols
“As a general practitioner with extensive experience in women’s health, I frequently encounter patients whose hormonal symptoms are dismissed or misattributed. This panel offers a structured biochemical assessment that helps differentiate treatable endocrine conditions from lifestyle or stress-related fluctuations. Always pair lab results with a thorough clinical evaluation before making any treatment decisions.” – Dr. Ajay Singh | General Practitioner | DHA Registration ID: 36234132
Medication Advisory
Do not discontinue any prescribed hormone therapy, oral contraceptives, or other medications without consulting your doctor. Abrupt cessation can cause serious adverse effects including menstrual irregularities, bone density loss, and cardiovascular complications.
Exclusion Criteria & Red Flags
Exclusion Criteria & Red Flags
- Known pregnancy or breastfeeding – panel interpretation is unreliable.
- Current use of GnRH agonists, high-dose corticosteroids, or biotin >5 mg/day (stop 48 hours before draw).
- Fever >38.5 °C or acute systemic illness – reschedule when clinically stable.
- Minors (<18 years): Valid guardian consent required per Federal Decree-Law No. 4 of 2016 on Medical Liability.
- ER Red Flags: Sudden severe pelvic pain, loss of consciousness, acute visual field defect – seek emergency care immediately; do not wait for test results.
Patient FAQ & Clinical Guidance
1. What does the female hypogonadism panel measure and when should I take it?
This panel measures pituitary hormones (FSH, LH, prolactin, TSH) and ovarian hormones (estradiol, AMH). For menstruating women, the preferred sample time is Day 2 or 3 of the cycle, taken in the morning. A 15-word summary: Measures pituitary and ovarian hormones to classify primary versus secondary hypogonadism in women.
2. How should I prepare for home collection and are any medications prohibited?
Fast for 8 hours (water allowed), avoid biotin supplements for 48 hours prior, and reschedule if you have an acute illness. Continue prescription medications unless your doctor advises otherwise. Key preparation: Fast 8 hours, withhold biotin 48 hours, and schedule collection on cycle Day 2-3.
3. What should I do if my results are abnormal?
Do not panic – abnormal values may be transient or related to sampling time. Our clinical support team provides a post-test tele-consult with an endocrinologist who will interpret your results in context. Contact our clinical team for a tele-consult with an endocrinologist to interpret abnormal values correctly.
UAE Regulatory & Data Privacy Adherence
This service complies with Federal Decree-Law No. 45 of 2021 on Personal Data Protection (PDPL) ensuring your health data remains confidential and secure. All laboratory testing adheres to Federal Law No. 2 of 2019 Concerning the Use of Information and Communication Technology in Health Fields, guaranteeing safe and ethical digital health practices. Results must be interpreted by a licensed physician. This panel is not a substitute for professional medical advice.
Clinical & Logistical Metadata
| Test Name | Female Hypogonadism Panel |
| Price (AED) | 850 |
| Turnaround Time | 3 working days |
| Sample Type / Matrix | Serum (2 mL from Red Top tube, No Additive) |
| Methodology Used | CLIA + LC-MS/MS |
| ICD-10-CM Code | E28.3 |
| LOINC Code | 101448-9 |
| DHA Facility License & Address | DHA License: 1143 | Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE | DNA Labs UAE |
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