We studied four patients affected by progressive myoclonic epilepsy: three patients had the clinical features of Lafora's disease while the fourth was affected by a Lundborg's type of myoclonic epilepsy. In all the above cases we found no specific electroencephalographic records of Lafora's disease; muscle histochemistry was useful for the diagnosis and the demonstration of PAS positive and NADH-TR positive Lafora's bodies. The authors discuss the nosographic situation of Lafora's body disease among the progressive myoclonic epilepsies.
Lafora's disease as a form of myoclonus epilepsy: 3 cases
Angelini C.
Membro del Collaboration Group
1980
Abstract
We studied four patients affected by progressive myoclonic epilepsy: three patients had the clinical features of Lafora's disease while the fourth was affected by a Lundborg's type of myoclonic epilepsy. In all the above cases we found no specific electroencephalographic records of Lafora's disease; muscle histochemistry was useful for the diagnosis and the demonstration of PAS positive and NADH-TR positive Lafora's bodies. The authors discuss the nosographic situation of Lafora's body disease among the progressive myoclonic epilepsies.File in questo prodotto:
Non ci sono file associati a questo prodotto.
Pubblicazioni consigliate
I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.
