Status Epilepticus as the Initial Manifestation of Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes Syndrome
Journal of the Korean Neurological Association
; : 276-280, 2020.
Article
en Ko
| WPRIM
| ID: wpr-834876
Biblioteca responsable:
WPRO
ABSTRACT
Mitochondrial encephalomyopathy with lactic acid and stroke-like episodes (MELAS) is a multisystem mitochondrial disorder that is rarely observed in adulthood. We report a case of MELAS syndrome diagnosed in a 22-year-old man presented with status epilepticus (SE) without a preceding stroke-like episode. Genetic testing revealed a mutation of heteroplasmic m.3243A>G. MELAS should be suspected in patients with recurrent, uncontrolled SE with unexplained severe lactic acidosis.
Texto completo:
1
Base de datos:
WPRIM
Idioma:
Ko
Revista:
Journal of the Korean Neurological Association
Año:
2020
Tipo del documento:
Article