Your browser doesn't support javascript.
loading
Recent research on the treatment of spinal muscular atrophy / 中国当代儿科杂志
Article in En | WPRIM | ID: wpr-928588
Responsible library: WPRO
ABSTRACT
Spinal muscular atrophy (SMA) is an autosomal recessive neuromuscular disease characterized by progressive muscular weakness and atrophy. SMA, as an inherited disease, is the leading cause of death in infants and young children. Rapid progress has been made in the research field of SMA in recent years, and some related treatment drugs have been successfully approved for marketing. This article reviews the recent research advances in the treatment of SMA.
Subject(s)
Key words
Full text: 1 Index: WPRIM Main subject: Muscular Atrophy, Spinal Limits: Child / Child, preschool / Humans / Infant Language: En Journal: Chinese Journal of Contemporary Pediatrics Year: 2022 Type: Article
Full text: 1 Index: WPRIM Main subject: Muscular Atrophy, Spinal Limits: Child / Child, preschool / Humans / Infant Language: En Journal: Chinese Journal of Contemporary Pediatrics Year: 2022 Type: Article