Complete Blood Count (CBC)
A blood test that measures the level of 17-hydroxyprogesterone, a hormone used to screen for and help diagnose congenital adrenal hyperplasia (CAH), a genetic condition affecting hormone production.
{"The test is primarily used for newborn screening to detect congenital adrenal hyperplasia (CAH)","CAH is a genetic disorder that affects the adrenal glands' ability to produce cortisol and aldosterone","Early detection through this test helps prevent serious health problems including salt-wasting crises and early puberty","The test is usually performed on a blood sample from a newborn's heel (heel stick)","Abnormal results require follow-up testing for confirmation and further evaluation"}
Key facts at a glance
- LOINC
- 38473-5
- Short code
- 17-OHP-DBS
- Synonyms
- 17OHP DBS-mCnc
- Category
- chemistry
- Sample
- serum
- Container
- Dried Blood Spot (DBS) filter paper collection card (e.g., Whatman 903 or equivalent)
- Units
- N/A
- Ref low
- 0
- Ref high
- 37
- Critical range
- — – 30 N/A
- Fasting
- false
- Population
- adult
- Sex
- all
- Age range
- 0–365 years
- Method
- Immunoassay (Chemiluminescence or ELISA) for Dried Blood Spot
- CPT
- 82157
- SNOMED
- 414268004
- Specimen volume
- 3-5 blood spots (approximately 75-100 μL total blood volume)
- Stability
- Room temperature: 7-14 days; Refrigerated (2-8°C): 30 days; Frozen (-20°C or below): 6-12 months. Protect from excessive heat and humidity.
- Hemolysis max
- 500
- Lipemia max
- 1000
- Icterus max
- 500
- TAT
- 24–72 hours
- Order
- routine
A complete blood count, or CBC, is a common blood test that measures the different cells in your blood, including red blood cells, white blood cells, and platelets. These cells carry oxygen, fight infection, and help your blood clot properly, so this test gives your doctor a broad picture of your overall health.
The 17-Hydroxyprogesterone (17-OHP) test measures the amount of a specific hormone called 17-hydroxyprogesterone in the blood. This hormone is produced by the adrenal glands, which sit on top of each kidney. The test is primarily used as a screening tool to detect a condition called congenital adrenal hyperplasia (CAH) in newborns, though it may also be used in older children and adults when CAH is suspected.
Your doctor may order a CBC as part of a routine checkup or to help investigate symptoms such as fatigue, weakness, fever, bruising, or unexplained bleeding. It is also used to monitor an ongoing condition or to check how a treatment, such as chemotherapy, is affecting your blood cells over time.
The main purpose of the 17-OHP test is to screen newborns for congenital adrenal hyperplasia (CAH). CAH is a group of genetic disorders that affect the adrenal glands' ability to produce cortisol, a stress hormone, and aldosterone, which helps regulate salt and water balance in the body. Without early detection and treatment, CAH can lead to serious complications including adrenal crisis, salt-wasting crises, abnormal puberty, and growth problems.
The test is done with a simple blood draw. A healthcare professional cleans a spot on your arm, usually the inside of your elbow, wraps a band around your upper arm, and collects a small sample of blood into a tube. The procedure takes only a few minutes, and you can return to your normal activities right afterward.
For newborns, a small blood sample is collected by pricking the baby's heel, similar to other routine newborn screening tests. The blood is placed on a special filter paper card and sent to a laboratory for analysis. In older children or adults, a blood sample is drawn from a vein in the arm. The test requires no special preparation such as fasting.
Your results show whether your blood cell counts fall within the normal range. High or low values can point to conditions such as anemia, infection, inflammation, or clotting problems. Your doctor will interpret the numbers together with your symptoms and medical history, since a single abnormal value does not always mean a serious problem.
Normal 17-OHP levels vary depending on the baby's age, weight, and whether they were born prematurely. Elevated levels of 17-OHP may indicate congenital adrenal hyperplasia, but further testing is needed to confirm the diagnosis. Very high levels are more likely to indicate classic CAH, while mildly elevated levels may require repeat testing or additional evaluation to rule out false positives or other conditions.
Reference range
Reference range varies by gestational age and birth weight. Typically: Premature infants (<37 weeks): <30 ng/mL; Term infants: <15 ng/mL; Most laboratories use <10 ng/mL as upper limit for term newborns. Values >30 ng/mL are highly suggestive of congenital adrenal hyperplasia (21-hydroxylase deficiency).N/A
No fasting required. Test is primarily performed on newborn screening specimens collected within 24-72 hours of life. For older children or adults, no special preparation needed. Inform clinician of any current steroid medications.
Clinical interpretation
How abnormal results are interpreted and what conditions they suggest.
The 17-OHP test is crucial for newborn screening programs worldwide. Congenital adrenal hyperplasia affects approximately 1 in 15,000 newborns worldwide. When detected early, CAH can be managed effectively with medication (usually hydrocortisone and sometimes fludrocortisone), allowing affected children to live healthy, normal lives. Without treatment, classic CAH can cause life-threatening salt-wasting crises in newborns and lead to premature puberty, rapid growth followed by short stature, and fertility problems in older children and adults.
The test is also valuable for diagnosing late-onset or non-classical CAH in older children and adults who may present with symptoms such as early puberty, hirsutism (excessive hair growth), irregular periods, or infertility. Genetic testing and additional hormone tests are typically used to confirm the diagnosis and determine the specific type of CAH.
Frequently asked questions
Is the 17-OHP test painful for my baby?
What happens if my baby's test result is abnormal?
Is CAH treatable?
Can CAH be detected before birth?
Is CAH inherited?
Sources
- 1
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- 4
Click any link to access the full source. PubMed Central (PMC) links provide free full-text access.
This information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.
This content is for general informational and educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment. Always seek the guidance of a qualified healthcare provider with any questions you have about a medical condition, and never disregard professional medical advice or delay seeking it because of something you read here.
If you think you may have a medical emergency, call your local emergency number or go to the nearest emergency department immediately.
Medically reviewed by WellAlly Editorial Team Last reviewed August 16, 2026. · Read our editorial policy