Research progresses on the cognitive impairment of Duchenne muscular dystrophy / 中华实用儿科临床杂志
Chinese Journal of Applied Clinical Pediatrics
;
(24): 954-957, 2022.
Artigo
em Chinês
| WPRIM
| ID: wpr-954670
ABSTRACT
Duchenne muscular dystrophy(DMD) is an X-linked hereditary neuromuscular disorder caused by dystrophin gene mutation.About 1/3 of DMD patients have cognitive impairment.Early detection of cognitive impairment is essential for early diagnosis and the quality of life.This review summarized the recent progress in the clinical features, pathogenesis, brain structure changes, and cognitive impairment intervention of DMD.
Texto completo:
DisponíveL
Índice:
WPRIM (Pacífico Ocidental)
Idioma:
Chinês
Revista:
Chinese Journal of Applied Clinical Pediatrics
Ano de publicação:
2022
Tipo de documento:
Artigo
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