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.
Article
in Chinese
| WPRIM (Western Pacific)
| ID: wpr-981973
Responsible library:
WPRO
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.
Full text:
Available
Database:
WPRIM (Western Pacific)
Main subject:
Quality of Life
/
Glycogen Storage Disease Type II
/
Alpha-Glucosidases
/
Enzyme Replacement Therapy
Limits:
Humans
Language:
Chinese
Journal:
Chinese Journal of Contemporary Pediatrics
Year:
2023
Document type:
Article