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ISBN 978-0-8385-1301-9

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Vitamin B6-dependent epilepsy is a group of autosomal recessive disorders caused by mutations in the genes for phosphatidylinositol binding protein (PLPBP), acetaldehyde dehydrogenase 4 family member A1 (ALDH4A1), acetaldehyde dehydrogenase 7 family member A1 (ALDH7A1), pyridoxal (amine) 5'-phosphate oxidase (PNPO), and tissue non-specific alkaline phosphatase (TNSALP)

As systemic metabolic function improves, secondary benefits such as enhanced muscle definition, improved skin tone, and overall physical refinement may be observed, reflecting improved cellular energy balance and reduced inflammatory burden

doi: 10.1111/bjh.12959

These tablets may work for some patients, but not all will derive any benefit, though why this is so is not yet understood..