Familial occurrence of myoclonic epilepsy syndrome and acute intermittent porphyria. Varsik P, Buranová D, Kollár B, Traubner P, Bozek P, Mikulecký M. Case Reports 2005; 26(1): 7-12 PubMed PMID: 15726012 Keywords: Adolescent, Adult, Anticonvulsants:therapeutic use, Brain:pathology, Child, Electroencephalography, Epilepsies, Myoclonic:complications, Female, Heme:therapeutic use, Humans, Hydroxymethylbilane Synthase:genetics, Male, Porphyria, Acute Intermittent:compl. Citation OBJECTIVES: Myoclonic epilepsy (ME) syndrome is not rare in north-eastern Europe; it is also seen in various forms. Familial occurrence of..... Read abstract Full text PDF