September 17, 2019


Keto Original Diet electrographic profile, thus suggesting a dissociation between the EEG and motor by pyruvate dehydrogenase deficiency, static encephalopathy, and seizure disorder was treated with KD and presented severe diabetic ketoacidosis. Pyruvate dehydrogenase deficiency is a rare genetic defect of mitochondrial energy metabolism that leads to inefficient glucose use and lactic acidosis. KD provides the brain with an alternate fuel source, but its implementation is in contrast with traditional diabetes management.

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