Galactosemia Newborn Screen Test

Introduction

The Galactosemia Newborn Screen Test is a vital diagnostic tool designed to identify galactosemia, an inborn error of metabolism that can lead to serious health complications if not detected early. This screening is typically performed shortly after birth, allowing for prompt intervention and management.

What the Test Measures

This test measures the levels of galactose in a newborn’s blood. Elevated levels can indicate galactosemia, which impairs the body’s ability to metabolize galactose, a sugar found in milk and dairy products.

Who Should Consider This Test

Parents should consider the Galactosemia Newborn Screen Test for their newborns, especially if there is a family history of metabolic disorders. Symptoms of galactosemia may include:

• Jaundice
• Vomiting
• Failure to thrive
• Sepsis

Early detection can prevent severe complications associated with the condition.

Benefits of Taking the Test

Taking the Galactosemia Newborn Screen Test offers numerous benefits, including:

• Early diagnosis and treatment to prevent serious health issues.
• Guidance on dietary restrictions to manage the condition effectively.
• Peace of mind for parents regarding their child’s health.

Understanding Your Results

Results from the Galactosemia Newborn Screen Test are typically available the next day. A healthcare provider will interpret the results, providing guidance on the next steps if elevated levels of galactose are detected. It’s essential to follow up with a pediatrician for further evaluation and management.

Test Pricing

Book the Test

To ensure the health and well-being of your newborn, book the Galactosemia Newborn Screen Test today! For inquiries or to schedule your appointment, please call or WhatsApp us at +2348077798758.

We are committed to providing accurate and timely diagnostic services to our patients. Trust DNA Labs Nigeria for your newborn’s health screenings.