G6PD deficiency is a genetic abnormality that results in an inadequate amount of glucose-6-phosphate dehydrogenase (G6PD) in the blood. This is a very important enzyme (or protein) that regulates ...

Glucose-6 phosphate dehydrogenase (G6PD) deficiency is a common inherited enzyme disorder that can cause hemolytic anemia, jaundice, dark red urine, and paleness. The best way to prevent symptoms is ...

In a recent study published in Nutrients, researchers investigated the risk of Attention Deficit/Hyperactivity Disorder (ADHD) among glucose 6-phosphate dehydrogenase (G6PD)-deficient individuals.

It's a blood test that measures the amount of glucose-6-phosphate dehydrogenase (G6PD) in your body. G6PD is an enzyme that helps your red blood cells work properly. If your G6PD level is too low, you ...

In an April 8 MedPage Today article, Mark Zucker, MD, asked the question as to why there is differential susceptibility to COVID-19 infection. In other words, why do some people become severely ill ...

G6PD deficiency is caused by mutations in the G6PD gene, which provides instructions for producing the G6PD enzyme. This enzyme plays a crucial role in protecting red blood cells from oxidative damage ...

On 18 December 2024, the World Health Organization (WHO) prequalified the first diagnostic test for glucose-6-phosphate dehydrogenase (G6PD) deficiency which can help to safely deliver WHO-recommended ...

A: G6PD deficiency is a very common inherited condition, affecting over 400 million people worldwide. It is more prevalent in those of African, Asian or Mediterranean decent; this could be because ...