[Research progress of nervous system damage in Pompe disease]. / åºè´ç
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Zhongguo Dang Dai Er Ke Za Zhi
; 25(4): 420-424, 2023 Apr 15.
Article
en Zh
| MEDLINE
| ID: mdl-37073849
ABSTRACT
Pompe disease, also known as glycogen storage disease type â
¡, 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.
Palabras clave
Texto completo:
1
Banco de datos:
MEDLINE
Asunto principal:
Enfermedad del Almacenamiento de Glucógeno Tipo II
Límite:
Humans
Idioma:
Zh
Revista:
Zhongguo Dang Dai Er Ke Za Zhi
Año:
2023
Tipo del documento:
Article
País de afiliación:
China