17 Hydroxyprogesterone Newborn Screen CAH Screen Test
Introduction to the Test
The 17 Hydroxyprogesterone Newborn Screen CAH Screen Test is a vital diagnostic tool used to detect congenital adrenal hyperplasia (CAH) in newborns. CAH is a genetic disorder that affects the adrenal glands, leading to a deficiency in cortisol production and an overproduction of androgens. Early detection through this screening can significantly improve health outcomes by allowing for prompt treatment and management.
What the Test Measures
This test measures the levels of 17 hydroxyprogesterone (17-OHP) in a newborn’s blood. Elevated levels of 17-OHP can indicate the presence of CAH, prompting further evaluation and potential intervention.
Who Should Consider This Test
Newborns, especially those with symptoms such as ambiguous genitalia or a family history of adrenal disorders, should undergo this screening. Additionally, infants exhibiting signs of adrenal insufficiency or hormonal imbalances may also be recommended for this test.
Benefits of Taking the Test
- Early detection of congenital adrenal hyperplasia.
- Prevention of severe health complications through timely intervention.
- Peace of mind for parents regarding their child’s health.
- Guides healthcare providers in managing hormonal disorders effectively.
Understanding Your Results
Results from the 17 Hydroxyprogesterone Newborn Screen CAH Screen Test are typically available within one week. A positive result may indicate the need for further testing and consultation with an endocrinologist or pediatrician to confirm the diagnosis and discuss treatment options.
Test Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| 17 Hydroxyprogesterone Newborn Screen CAH Screen Test | 5850 NGN | 6500 NGN |
Book the Test
Ensure the health of your newborn by booking the 17 Hydroxyprogesterone Newborn Screen CAH Screen Test today! For appointments, please call or WhatsApp us at +2348077798758. Early detection is key to effective management of potential health issues.
Test Details
- Turnaround Time: 1 week
- Sample Type: 1 drop of heel prick blood each on 3 spots of filter paper available from LPL. Ship refrigerated or frozen. Clinical details and drug history must accompany the sample.
- Pre-Test Instructions: Clinical details and drug history must accompany the sample.
- Specialty: Endocrinologist, Pediatrician
- Department: Genetic
- Method: Fluoroimmunoassay
- Disease Type: Genetic Disorders
