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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)
Accessed July 15, 2025
research compound only Product Specifications Format: lyophilized powder in vial (reconstitute with bacteriostatic water) Strengths available: 10 mg per vial
10.1038/s41387-018-0017-1 19
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