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Up to: Hereditary neurological disease · Metabolic epilepsy · Inborn disorder of pyridoxine metabolism

Pyridoxal phosphate-responsive seizures

A very rare neonatal epileptic encephalopathy disorder characterized clinically by onset of severe seizures within hours of birth that are not responsive to anticonvulsants, but are responsive to treatment with pyridoxal phosphate.

2 trials tagged with this condition →

This condition has no sub-types.