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Up to: Hereditary neurological disease · Metabolic epilepsy · Inborn disorder of pyridoxine metabolism
Pyridoxine-dependent epilepsy
A rare neurometabolic disease characterized by recurrent intractable seizures in the prenatal, neonatal and postnatal period that are resistant to anti-epileptic drugs (AEDs) but that are responsive to pharmacological dosages of pyridoxine (vitamin B6).