Research progress of nervous system damage in Pompe disease / 中国当代儿科杂志
Chinese Journal of Contemporary Pediatrics
;
(12): 420-424, 2023.
Artigo
em Chinês
| WPRIM
| ID: wpr-981973
ABSTRACT
Pompe disease, also known as glycogen storage disease type Ⅱ, is a rare autosomal recessive disease. With the application of enzyme replacement therapy, more and more patients with Pompe disease can survive to adulthood, and nervous system-related clinical manifestations gradually emerge. Nervous system involvement seriously affects the quality of life of patients with Pompe disease, and a systematic understanding of the clinical manifestations, imaging features and pathological changes of nervous system injury in Pompe disease is of great significance for the early identification and intervention of Pompe disease. This article reviews the research progress of neurological damage in Pompe disease.
Texto completo:
DisponíveL
Índice:
WPRIM (Pacífico Ocidental)
Assunto principal:
Qualidade de Vida
/
Doença de Depósito de Glicogênio Tipo II
/
Alfa-Glucosidases
/
Terapia de Reposição de Enzimas
Limite:
Humanos
Idioma:
Chinês
Revista:
Chinese Journal of Contemporary Pediatrics
Ano de publicação:
2023
Tipo de documento:
Artigo
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