| Literature DB >> 3627423 |
K Hasuo, S Tamura, K Yasumori, A Uchino, S Goda, S Ishimoto, K Kamikaseda, Y Wakuta, M Kishi, K Masuda.
Abstract
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.Entities:
Mesh:
Year: 1987 PMID: 3627423 DOI: 10.1007/BF00348922
Source DB: PubMed Journal: Neuroradiology ISSN: 0028-3940 Impact factor: 2.804