A Case of Early Onset MELAS Patient with Wolff-Parkinson-White Syndrome / 대한소아신경학회지
Journal of the Korean Child Neurology Society
;
(4): 266-271, 2011.
Artigo
em Inglês
| WPRIM
| ID: wpr-32905
ABSTRACT
Mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome is one of the classic mitochondrial diseases characterized by symptoms of repeated episodes of hemiparesis with mitochondrial DNA mutation. We report a rare case of early onset MELAS patient confirmed by genetic analysis with Wolff-Parkinson-White syndrome.
Texto completo:
DisponíveL
Índice:
WPRIM (Pacífico Ocidental)
Assunto principal:
Paresia
/
Síndrome de Wolff-Parkinson-White
/
Acidose Láctica
/
DNA Mitocondrial
/
Miopatias Mitocondriais
/
Encefalomiopatias Mitocondriais
/
Síndrome MELAS
/
Doenças Mitocondriais
Limite:
Humanos
Idioma:
Inglês
Revista:
Journal of the Korean Child Neurology Society
Ano de publicação:
2011
Tipo de documento:
Artigo
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