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G6PD Deficiency: What It Is and Why Do Newborns Need Screening For It?

Olivia Barredo
October 27, 2022


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Get to know more about G6PD deficiency and why it’s important to have your baby test screened! 

 

What is G6PD Deficiency?

 

 

As per Baby’s First test, a G6PD deficiency or (Glucose-6-phosphate dehydrogenase deficiency) is an inherited condition of the blood where no signs or symptoms of conditions are being shown until they are exposed to foods, infections, or certain medications. 

 

The signs and symptoms of G6PD deficiency include:

 

  • Shortness of breath & rapid heart rate

  • Exhaustion or easily tired 

  • Paleness

  • Yellow skin tone 

  • Abnormal urine color (Dark urine)



Why Do Newborns Need to be Screened for G6PD Deficiency?

 

G6PD deficiency can result in life-threatening reactions and neonatal jaundice and to several foods, infections, and medications, so it is essential to have newborns undergo test screenings. 

 



Possible Treatments for G6PD Deficiency 

 

As prescribed by a nutritionist or dietician, infants may need to undergo a dietary treatment which means - planning a healthy diet for your baby and a way of avoiding chemicals that cause destroyed red blood cells. 



Have your baby test screened now!