Hasuo K, Tamura S, Yasumori K, Uchino A, Goda S, Ishimoto S, Kamikaseda K, Wakuta Y, Kishi M, Masuda K
Neuroradiology. 1987;29(4):393-7. doi: 10.1007/BF00348922.
Among mitochondrial encephalomyopathies, MELAS (mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes, Pavlakis et al. 1983) is recognized as a distinct syndrome characterized by generalized convulsions and recurrent stroke-like episodes. The neuroradiological findings of three patients with MELAS are reported here. Retrospective review shows that MELAS should be included in the differential diagnosis of infarct-like lesions of the cerebrum.