MELAS syndrome

P. Montagna, R. Gallassi, R. Medori, E Govoni, Massimo Zeviani, S. Di Mauro, E Lugaresi, Frédérick Andermann

Neurology · 1988 · 182 citations · 0 references

Concepts

Abstract

Severe prolonged migrainous symptoms and prolonged partial status epilepticus are characteristic features of the MELAS syndrome (mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes). Maternal transmission previously found in myoclonus epilepsy and ragged-red fibers (MERRF), another mitochondrial disease, is suggested in this disorder as well.