Prenatal & Fertility Tests
About Prenatal & Fertility Tests
Our comprehensive range of Prenatal & Fertility tests are designed to provide accurate insights into your health. We partner with the best labs in UAE to ensure reliable results.
Available Tests

17-ALPHA HYDROXYPROGESTERONE (NEONATAL SCREENING) Test in UAE
17-Alpha Hydroxyprogesterone (Neonatal Screening) test in Dubai and across the UAE to detect congenital adrenal hyperplasia (CAH) in newborns. This life-saving screening helps identify babies at risk of hormonal imbalances, adrenal crisis, or genital abnormalities. Results available within 5–10 days.
Overview
The 17-Alpha Hydroxyprogesterone (17-OHP) Neonatal Screening test is a critical part of newborn screening programs in the UAE. It measures 17-OHP levels in a dried blood spot to detect 21-hydroxylase deficiency — the most common form of congenital adrenal hyperplasia (CAH). Early detection allows immediate treatment to prevent life-threatening adrenal crises, electrolyte imbalances, and developmental issues. Results are typically available within 5–10 days.
Why You Need This Test
- Early detection of congenital adrenal hyperplasia (CAH) before symptoms appear.
- Prevent adrenal crisis (vomiting, dehydration, shock) in newborns with salt-wasting CAH.
- Identify babies at risk of ambiguous genitalia (especially in genetic females).
- Mandatory screening in many UAE hospitals between day 2 and day 5 of life.
- Support early intervention with hormone replacement and monitoring.
- Part of a comprehensive newborn metabolic screening panel.
- Available for home follow-up testing if initial screening was delayed.
Symptoms & Risk Factors
Common Signs (if untreated)
- Poor feeding, vomiting, or weight loss in the first week of life.
- Dehydration, low sodium, high potassium — signs of salt-wasting crisis.
- Darkened skin (hyperpigmentation) due to high ACTH.
- Genital abnormalities in genetic females (enlarged clitoris, fused labia).
- Low blood sugar or lethargy.
Risk Factors
- Family history of congenital adrenal hyperplasia (CAH).
- Consanguineous parents (increased genetic risk).
- Previous child diagnosed with CAH in the family.
- Not screened at birth — late or missed newborn screening.
- Preterm infants: may have transiently elevated 17-OHP (requires follow-up).
How the Test Works
The test measures 17-alpha-hydroxyprogesterone (17-OHP) — a hormone that builds up when the adrenal gland can't make cortisol due to enzyme deficiency.
- Step 1 — Timing: ideally performed between the 2nd and 5th day of life (after full feeding).
- Step 2 — Sample collection: a small blood sample is taken via heel prick and blotted onto a filter paper card (dried blood spot).
- Step 3 — Documentation: a complete Clinical History form must accompany the sample, including birth date, birth time, feeding status, and gestational age.
- Step 4 — Lab analysis: specialized immunoassay measures 17-OHP levels.
- Step 5 — Results: delivered securely within 5–10 business days.
This non-invasive test is a cornerstone of preventive pediatric care in the UAE.
Specimen (Sample Type)
- Required sample: Dried Blood Spot (DBS) from heel prick
- Collection window: ideally between Day 2 and Day 5 of life
- Form required: completed Clinical History form (birth date, birth time, feeding, gestational age)
- Handling: avoid touching or smearing the blood spots — use clean hands and proper technique
- Drying: air-dry horizontally for a minimum of 3 hours
- Transport: ship to the lab as soon as dry, and no later than 24 hours after collection
- Note: improperly handled or delayed specimens may be rejected
Risks & Safety
- Minimal discomfort: brief pinch during heel prick.
- Small bruise or redness at the site — resolves quickly.
- No infection risk when sterile lancets are used.
- No long-term risks — this is a standard, safe screening procedure.
Result Interpretation
Normal Range
- Term infants: usually < 200 ng/dL (lab-dependent cutoff)
- Levels vary by age, birth weight, and time of collection
Elevated Levels
- May indicate:
- Classic 21-hydroxylase deficiency (CAH)
- Non-classic CAH (milder form)
- Preterm birth (transient elevation)
- Stress or illness in newborn period
- Abnormal screen requires urgent follow-up with serum 17-OHP, cortisol, and electrolytes.
False Positives
- More common in preterm, low birth weight, or sick infants.
- Requires repeat testing to confirm.
Consequences if Untreated
- Adrenal crisis: vomiting, dehydration, shock, death within days.
- Electrolyte imbalance: low sodium, high potassium, cardiac arrhythmias.
- Permanent genital abnormalities in undiagnosed genetic females.
- Delayed diagnosis increases risk of hospitalization and long-term complications.
Factors Affecting Test Results
- Timing: testing too early (<24h) or too late (>5 days) reduces accuracy.
- Birth weight: preterm infants often have higher 17-OHP.
- Feeding status: must be fed before testing — affects hormone levels.
- Stress or illness: can elevate 17-OHP temporarily.
- Sample handling: touching, smearing, or delayed transport affects reliability.
FAQs
When is the 17-OHP neonatal test done?
Between the 2nd and 5th day of life, after the baby has been adequately fed.
Is this test mandatory in the UAE?
Yes. It is part of the recommended newborn screening panel in most hospitals across Dubai and the Emirates.
How is the sample collected?
Through a heel prick — a few drops of blood are placed on a filter paper card to create a dried blood spot (DBS).
What is the Clinical History form?
A mandatory form that includes birth date, birth time, feeding method, gestational age, and clinical notes — essential for accurate interpretation.
Can this test be done at home?
Yes. If your baby missed the hospital screening, we offer home neonatal screening with a trained pediatric nurse.
How long for results?
Results are typically available within 5–10 days after the lab receives the properly dried and transported sample.
What is the price of the test?
The 17-Alpha Hydroxyprogesterone (Neonatal) test costs AED 150 in the UAE, including home collection if needed.
Limitations
- Not 100% diagnostic — elevated results require confirmatory serum testing.
- May miss non-classic or late-onset CAH (use serum test for older children).
- Higher false positive rate in preterm or ill newborns.
- Strict collection and transport rules — improper handling leads to sample rejection.
- Must be collected within the 2nd–5th day window for optimal accuracy.
Book Your 17-Alpha Hydroxyprogesterone (Neonatal Screening) Test Today
Protect your baby’s health from day one — early detection saves lives.
- Home Neonatal Screening Available (Across Abu Dhabi, Dubai, Sharjah, Ajman, RAK, Umm Al Quwain, Fujairah)
- Fast, Accurate, Confidential Results in 5–10 Days
- Price: AED 150
- ✅ Certified Labs | Newborn Screening Accredited
- 👶 Trained Pediatric Nurses for Home Collection
- 🔒 Secure Reporting & Doctor Support

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NIPT - Basic (NON- CE IVD) Trisomy 21, 18, 13, Sex chromosome abnormalities and Gender
NIPT - Basic (NON-CE IVD) | Test for Trisomy 21, 18, 13, Sex Chromosome Abnormalities & Gender
The Non-Invasive Prenatal Test (NIPT) - Basic (NON-CE IVD) screens for common chromosomal abnormalities including:
- - Trisomy 21 (Down Syndrome)
- - Trisomy 18
- - Trisomy 13
- - Sex chromosome abnormalities
- - Fetal gender determination
This test uses just 10 mL of maternal blood, collected in a special tube provided by Lifenity. It is valid from 10 weeks of gestation onwards.
Why You Need This Test
NIPT is an essential screening for expecting parents seeking peace of mind about their baby’s health. It is:
- - Non-invasive and safe for both mother and baby
- - Highly accurate for detecting genetic disorders
- - Performed early in pregnancy (from 10 weeks)
- - A powerful alternative to riskier invasive tests like amniocentesis
Symptoms or Risk Factors That Indicate the Need for This Test
- - Mother’s age is 35 years or older
- - Abnormal findings on a prenatal ultrasound
- - Family history of genetic or chromosomal disorders
- - Positive results from first-trimester screenings
- - Previous pregnancy affected by chromosomal conditions
Understanding Natural Fetal Chromosome Development
Most pregnancies result in a typical number of chromosomes, but errors can occur during fetal development. These errors may lead to conditions such as:
- - Down Syndrome (Trisomy 21)
- - Edwards Syndrome (Trisomy 18)
- - Patau Syndrome (Trisomy 13)
- - Sex chromosome abnormalities like Turner or Klinefelter syndrome
NIPT analyzes fetal DNA from the mother's blood, providing early detection with high accuracy and no risk to the fetus.
What Happens If It Goes Undiagnosed?
- - Potential emotional and medical distress later in pregnancy
- - Lack of preparedness for medical care or interventions at birth
- - Increased difficulty in making informed decisions
- - Delayed access to genetic counseling or supportive care
Early screening allows timely action and better prenatal care planning.

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