Short Description

This test should be used in neonates to screen for thyroid disease and G6PD deficiency.

PreTest Information

Clinical details and drug history must accompany sample.

Detail Description

Newborn Screening Panel 2 Test: Symptoms, Diagnosis, and Cost

As a parent, you want to do everything possible to ensure the health and well-being of your newborn. This includes making sure that they receive the necessary medical tests and screenings, such as the Newborn Screening Panel 2 Test.

The Newborn Screening Panel 2 Test is a comprehensive screening that checks for a variety of genetic disorders that may not be immediately apparent at birth. These disorders can cause serious health problems if left undiagnosed and untreated, so early detection is crucial.

Symptoms and Diagnosis

Many of the genetic disorders that the Newborn Screening Panel 2 Test screens for do not have obvious symptoms at birth. However, if your baby does exhibit any of the following symptoms, it's important to consult with a healthcare provider as soon as possible:

• Difficulty feeding or gaining weight
• Abnormal urine or stool
• Jaundice (yellowing of the skin or eyes)
• Seizures
• Lethargy or decreased activity

The Newborn Screening Panel 2 Test is typically performed within the first few days of life, before leaving the hospital. It involves a simple blood test, which is sent to a laboratory for analysis. Results are typically available within a few weeks.

Cost

The cost of the Newborn Screening Panel 2 Test varies depending on the laboratory and location. In India, the average cost of the test is INR 585. While this may seem like a significant expense, the benefits of early detection and treatment of genetic disorders far outweigh the cost.

Many insurance plans cover the cost of the Newborn Screening Panel 2 Test, so it's important to check with your provider to see if you're covered. Additionally, some hospitals may offer the test at a reduced cost or for free.

Conclusion

The Newborn Screening Panel 2 Test is a crucial screening that can help detect genetic disorders early, before they cause serious health problems. If you're a new parent, it's important to talk to your healthcare provider about the test and ensure that your baby receives it within the first few days of life.

Remember, early detection and treatment can make all the difference in your child's health and well-being.