G6PD Newborn Screen Test

Introduction

The G6PD Newborn Screen Test is a vital diagnostic procedure that screens newborns for Glucose-6-Phosphate Dehydrogenase (G6PD) deficiency, a genetic condition that can lead to hemolytic anemia and other serious health issues if not identified early. This test is crucial for ensuring the well-being of infants, particularly in populations where G6PD deficiency is prevalent.

What the Test Measures

This test measures the levels of G6PD enzyme in the blood. The absence or deficiency of this enzyme can result in the destruction of red blood cells, leading to anemia and other complications. Early detection allows for timely intervention.

Who Should Consider This Test

All newborns should undergo the G6PD Newborn Screen Test, especially those:

• With a family history of G6PD deficiency or related genetic disorders.
• Exhibiting symptoms such as jaundice, fatigue, or unusual paleness.

The test is particularly important for infants in high-risk populations.

Benefits of Taking the Test

• Early detection of G6PD deficiency, allowing for prompt medical management.
• Prevention of complications such as severe anemia and jaundice.
• Peace of mind for parents, knowing their child’s health status.

Understanding Your Results

Results from the G6PD Newborn Screen Test are typically available the next day. A normal result indicates sufficient enzyme levels, while a low result suggests G6PD deficiency. It is essential to consult with a pediatrician to understand the implications of your child’s results and discuss potential management strategies.

Test Pricing

Convenient Testing Across Kenya

We have branches across all major cities in Kenya, ensuring that you can access this essential test with ease. For your convenience, we also offer home sample collection services. To book the G6PD Newborn Screen Test, please call or WhatsApp us at +254711564616.

Ensure your newborn’s health today by scheduling this important screening test!