A Case of Adult Onset Glycogen Storage Myopathy / 대한임상신경생리학회지
Korean Journal of Clinical Neurophysiology
; : 81-85, 2014.
Article
em Ko
| WPRIM
| ID: wpr-208475
Biblioteca responsável:
WPRO
ABSTRACT
Primary metabolic myopathy as a type of congenital myopathies was first described by McArdle in 1951. Glycogen storage disease is a disease caused by genetic mutations involved in glycogen synthesis, glycogenolysis or glycolysis. Several types of glycogen storage disease are known to cause metabolic myopathies. We report a case of adult onset metabolic myopathy with glycogen storage.
Palavras-chave
Texto completo:
1
Índice:
WPRIM
Assunto principal:
Doença de Depósito de Glicogênio
/
Glicogenólise
/
Glicogênio
/
Glicólise
/
Doenças Musculares
Limite:
Adult
/
Humans
Idioma:
Ko
Revista:
Korean Journal of Clinical Neurophysiology
Ano de publicação:
2014
Tipo de documento:
Article