Test Price
700 AED✅ Home Collection Available
Amenorrhoea Profile Test in Dubai | 700 AED | DHA Licensed Lab
Executive Summary & Core Metrics
Key Highlights
- 99.9% Diagnostic Accuracy: Validated via ISO 9001:2015 certified laboratory processing (Cert: INT/EGQ/2509DA/3139).
- VIP Mobile Phlebotomy & Temperature-Controlled Cold-Chain Home Collection: Available daily from 8 AM to 11 PM. Our accredited phlebotomists ensure sterile, low-stress sample acquisition at your residence.
- Clinical Consultation: A telephonic interpretation of your results by a DHA-licensed general practitioner is included after reporting.
- Insurance Verification: Direct coverage check via WhatsApp: +971 54 548 8731.
- DHA Facility License: 1143 | Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE.
Test Overview & Methodology
The Amenorrhoea Profile is a focused hormonal blood panel that measures key reproductive and metabolic hormones to diagnose the endocrine causes of missed menstrual periods. It helps clinicians differentiate between ovarian, pituitary, and thyroid dysfunctions, enabling targeted treatment for fertility restoration or symptom management.
| Feature | Our Amenorrhoea Profile | Standard Lab Test |
|---|---|---|
| Methodology | Chemiluminescent Immunoassay (high sensitivity) | Often basic immunoassay without third-generation precision |
| Turnaround Time | Daily (results within 24 h) | 2–5 working days |
| Home Collection | ✅ ISO‑certified cold‑chain mobile phlebotomy | ❌ Clinic visit only |
| Post‑Test Consultation | Telephonic specialist interpretation | Rarely included |
| Accreditation | ISO 9001:2015 (Cert: INT/EGQ/2509DA/3139) | May lack international quality mark |
| Price | 700 AED | Variable, often higher when combined with consultation |
Physician Insight & Safety Protocols
Dr. Ajay Singh (General Practitioner, DHA Registration ID: 36234132) shares:
“Amenorrhoea is a clinical sign, not a final diagnosis. This targeted profile provides the biochemical roadmap to differentiate between common endocrine disruptions—such as polycystic ovary syndrome, hyperprolactinemia, and thyroid dysfunction—that can silence the menstrual cycle. However, results must always be integrated with a detailed clinical history and, when indicated, pelvic imaging. A normal hormone panel does not exclude all pathology, and every value should be interpreted in the context of the patient’s complete reproductive narrative.”
Important Advisory: Medication & Supplement Interference
⚠️ Critical Note: Do not discontinue any prescribed medication, including hormonal contraceptives, without consulting your physician. Blood levels of certain hormones can be significantly altered by supplements such as biotin. Disclose all prescription drugs, over-the-counter products, and herbal supplements to your phlebotomist at the time of collection to ensure result accuracy.
Exclusion Criteria & Emergency Red Flags
- Exclusion Criteria: Known pregnancy, acute febrile illness, untreated severe hypothyroidism or hyperthyroidism (unstable), recent use of gonadotropin-releasing hormone analogues (e.g., Zoladex, Lupron), current chemotherapy.
- Pre‑test Requirements: Overnight fasting is preferred; sample must be drawn 4 hours after waking. Avoid biotin supplements for 72 hours; intense exercise and significant emotional stress should be postponed for 24 hours.
- Red Flags (seek emergency care immediately): Sudden, severe pelvic/abdominal pain with dizziness; acute visual field loss or severe headache suggesting pituitary apoplexy; suicidal ideation together with amenorrhoea in the context of depression; blood pressure >180/120 mmHg.
Patient FAQ & Clinical Guidance
1. What is included in an Amenorrhoea Profile, and why is it needed for missed periods?
Snippet: A comprehensive hormone panel measuring FSH, LH, prolactin, estradiol, and TSH to diagnose endocrine causes.
The profile typically quantifies follicle‑stimulating hormone (FSH), luteinizing hormone (LH), prolactin, estradiol, and thyroid‑stimulating hormone (TSH) in a single blood draw. It is the first‑line biochemical screen to identify ovarian insufficiency, hyperprolactinemia, hypothalamic dysfunction, or thyroid abnormalities that can interrupt menstrual cycles.
2. How should I prepare for this blood test to ensure accurate results?
Snippet: Overnight fasting and blood collection 4 hours after waking are required for baseline hormone assessment.
Collect the blood sample exactly 4 hours after you have awakened from a typical night’s sleep; overnight fasting (water is allowed) helps stabilise prolactin and glucose‑sensitive hormones. Avoid heavy physical activity, emotional stress, and biotin‑containing supplements for 24–72 hours before the draw. Our phlebotomist will confirm these details during home collection.
3. Can this identify the root cause of amenorrhoea?
Snippet: It identifies endocrine abnormalities like hyperprolactinemia or ovarian insufficiency but may need imaging for structural causes.
The profile highlights hormonal imbalances that explain the majority of amenorrhoea cases; however, it does not visualise the reproductive anatomy. If results suggest hypothalamic‑pituitary disruption or if initial treatment fails, your gynaecologist may add an MRI and pelvic ultrasound. Always interpret these results together with your full medical history.
UAE Regulatory & Data Privacy Adherence
This diagnostic service operates in full compliance with the UAE’s highest data protection and health information security standards. Your personal health data is protected under 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. All clinical testing safety and patient consent procedures adhere to Federal Decree-Law No. 4 of 2016 on Medical Liability. DNA Labs UAE ensures that all laboratory processes are ISO 9001:2015 certified, guaranteeing the integrity and confidentiality of your medical information.
Clinical & Logistical Metadata
| Test Name | Amenorrhoea Profile |
| Price (AED) | 700 AED |
| Turnaround Time | Daily (results within 24 hours) |
| Sample Type / Matrix | Peripheral Whole Blood (Serum) |
| Methodology Used | Chemiluminescent Immunoassay (CLIA) |
| ICD-10-CM Code | N91.2 |
| LOINC Code | 24318-2 |
| DHA Facility License & Laboratory Address | License: 1143 | Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE | DNA Labs UAE |
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