Neonatal Screening (17- Alpha Hydroxyprogesterone) - Test Price | Sprint Diagnostics Hyderabad

Patient Preparing : The Neonatal Screening for 17-Alpha Hydroxyprogesterone (17-OHP) is a crucial test for newborns to identify the presence of Congenital Adrenal Hyperplasia (CAH), a group of inherited disorders that affect the adrenal glands. This specific screening is aimed at identifying elevated levels of 17-OHP, a hormone that is typically increased in individuals with CAH. The early detection of this condition through neonatal screening can enable prompt treatment, which can significantly improve the infant's health and long-term prognosis.

₹ 450


The Neonatal Screening for 17-Alpha Hydroxyprogesterone (17-OHP) is a crucial test for newborns to identify the presence of Congenital Adrenal Hyperplasia (CAH), a group of inherited disorders that affect the adrenal glands. This specific screening is aimed at identifying elevated levels of 17-OHP, a hormone that is typically increased in individuals with CAH. The early detection of this condition through neonatal screening can enable prompt treatment, which can significantly improve the infant's health and long-term prognosis.

Test Name Neonatal Screening (17- Alpha Hydroxyprogesterone)
Sample Type Heel Prick Dried Blood Spot
Preparations Required The Neonatal Screening for 17-Alpha Hydroxyprogesterone (17-OHP) is a crucial test for newborns to identify the presence of Congenital Adrenal Hyperplasia (CAH), a group of inherited disorders that affect the adrenal glands. This specific screening is aimed at identifying elevated levels of 17-OHP, a hormone that is typically increased in individuals with CAH. The early detection of this condition through neonatal screening can enable prompt treatment, which can significantly improve the infant's health and long-term prognosis.
Report Time 3 Days
Price in Hyderabad ₹ 450

What does the neonatal screening test for?

This screening test helps detect seven different conditions: Congenital Hypothyroidism, Congenital Adrenal Hyperplasia (CAH), Glucose-6-phosphate dehydrogenase (G6PD) deficiency, Cystic Fibrosis, Phenylketonuria, Galactosemia, and Biotinidase deficiency. Early diagnosis of these conditions can greatly improve a child's quality of life and long-term health.

How is the screening test performed?

The screening test is performed using a heel prick procedure, in which a small puncture is made in the baby's heel to obtain a few drops of blood. The blood sample is collected on a special filter paper and sent to a laboratory for further testing.

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Why is it important to screen for these conditions?

These conditions, if undetected and untreated, can cause serious health problems, including developmental delays, physical disabilities, and in severe cases, life-threatening situations. Early detection enables prompt treatment and intervention, significantly improving the child's prognosis.

When should this test be performed?

The test is usually performed within the first few days of the newborn's life. The exact timing can vary based on the hospital's policy and the health condition of the newborn.

Is the test painful for the newborn?

The heel prick might cause a moment of discomfort for the baby, but it is generally well-tolerated. The pain is temporary, and the health benefits of early detection far outweigh the brief discomfort.

What do positive test results mean?

A positive result indicates a high likelihood that the newborn has one of the tested conditions. However, a positive result is not a definitive diagnosis, and additional tests are necessary to confirm the result.

What do negative test results mean?

A negative result suggests that the baby likely does not have any of the conditions tested for. However, it's crucial to understand that this test does not screen for all possible health conditions, and regular pediatric check-ups are necessary to ensure the baby's overall health.

How accurate is the neonatal screening test?

The neonatal screening test is highly accurate. However, as with any test, there is always a chance of false positives or negatives. That's why a positive result is always followed up with more specific diagnostic tests.

What happens if the test results come back positive?

If the results are positive, additional diagnostic tests are necessary to confirm the diagnosis. If the diagnosis is confirmed, your doctor will guide you through the treatment and management options. The early detection allows for timely intervention, which can significantly improve the child's health outcome.

Are there any risks associated with the test?

There are minimal risks associated with this test. The heel prick may cause brief discomfort to the baby, and there may be slight bruising at the puncture site. However, these risks are minor compared to the benefit of detecting a potentially serious condition early.

Can the baby eat and drink before the test?

Yes, there are no specific dietary restrictions for this test. However, feeding patterns may impact some results, so it is crucial to follow the advice of your healthcare provider.

What are the treatments for these conditions?

The treatments vary for each condition. They might include special diets, medications, hormone replacement therapy, and in some cases, surgery. It's important to remember that early detection and management can significantly improve the child's health outcome.

Can these conditions be prevented?

Most of these conditions are genetic, meaning they cannot be prevented. However, with early detection and appropriate treatment, many of the symptoms and complications can be managed or even prevented.

Can my baby be tested at home?

The sample collection can be done at home, under the guidance of a healthcare professional. The samples are then sent to a laboratory for analysis.

How long will it take to receive the results?

Typically, you can expect to receive the results within 7 to 10 days after the sample has been received in the lab. However, the timeframe may vary depending on the specific lab and test.

Neonatal screening tests are vital for early detection of potentially life-altering conditions. This specific panel tests for seven conditions that, if undetected and untreated, can cause severe health complications. It's important to remember that these tests are screening tools and a positive result should be followed by confirmatory testing. As always, consult with your healthcare provider if you have any questions or concerns about your baby's health.

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