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The discovery of G6PD crystal structures and subsequent analyses provided us with further insights into this enzyme deficiency, since specific mutations can now be plotted on a 3D position in the protein structure

The disorder usually presents in early childhood and is characterized by episodes of hypoketotic hypoglycemia (that can cause encephalopathy), hepatomegaly, elevated liver enzymes (transaminases), and hypoammonemia in infants

If those muscles are not coordinating properly, no amount of fiber, water, or magnesium will produce a satisfying bowel movement

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These symptoms may signal vitreous hemorrhage, retinal detachment, or another urgent retinal complication