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Case reports have also indicated beneficial effects of KD in epileptic encephalopathies such as Lafora body disease (69), early infantile epileptic encephalopathy (70), LandauKleffner syndrome (71), subacute sclerosing panencephalitis (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)
Berglund LM, Lyssenko V, Ladenvall C, Kotova O, Edsfeldt A, Pilgaard K, et al
At 5 mg/mL, 40 units delivers 2 mg
A vial that passes visual inspection may still have lost potency
Mol Biol Evol 27, 395407, doi: 10.1093/molbev/msp251 (2010)
