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Figure 2 5.2 The ketogenic diet is beneficial for neuronal diseases and could be greatly influenced by precision medicine KD has been recommended for the treatment of certain epileptic and genetic syndromes including Dravet syndrome (72), adenylosuccinate lyase deficiency (73), juvenile myoclonic epilepsy (74), CDKL5 encephalopathy (75), infantile epilepsy with migrating focal seizures (76), childhood absence epilepsy (77), and epileptic encephalopathy with continuous spike-and-wave during sleep (78)
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A 42-year-old man dealing with fatigue and weight gain receives a different treatment plan than a 50-year-old athlete focused on recovery and performance, which is why men see meaningful results within 8 to 12 weeks rather than chasing generic protocols that never quite work
