Aucte intermittent porphyria and epilepsy.

A 14-year-old boy had suffered from intermittent acute hepatic porphyria, myoclonic convulsions and mental retardation (Lennox-Gastaut syndrome). The porphyria was treated by stopping the administration of phenobarbitone and phenytoin. Sodium valproate at a dose of 70 mg/kg per day lessened the severity and frequency of convulsive crises.

[1]  M. Brodie,et al.  Hereditary coproporphyria and epilepsy. , 1977, Archives of disease in childhood.

[2]  B. Grandchamp,et al.  The spectrophotometric determination of uroporphyrinogen I synthetase activity. , 1976, Clinica chimica acta; international journal of clinical chemistry.

[3]  N. Barclay Acute intermittent porphyria in childhood. A neglected diagnosis? , 1974, Archives of disease in childhood.

[4]  G. Stathers,et al.  Hereditary Coproporphyria: Study of a Swedish Family , 1968 .

[5]  R. I. Birchfield,et al.  Acute intermittent porphyria with seizures. Anticonvulsant medication-induced metabolic changes. , 1966, American journal of diseases of children.