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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.
Article Dans Chinois | 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.

Texte intégral: Disponible Indice: WPRIM (Pacifique occidental) langue: Chinois Texte intégral: Chinese Journal of Applied Clinical Pediatrics Année: 2022 Type: Article

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Texte intégral: Disponible Indice: WPRIM (Pacifique occidental) langue: Chinois Texte intégral: Chinese Journal of Applied Clinical Pediatrics Année: 2022 Type: Article