Pharmacological therapies for muscular dystrophies

被引:17
作者
Abdel-Hamid, Hoda [2 ]
Clemens, Paula R. [1 ,3 ]
机构
[1] Univ Pittsburgh, Dept Neurol, Pittsburgh, PA 15213 USA
[2] Univ Pittsburgh, UMPC, Childrens Hosp Pittsburgh, Div Neurol,Dept Pediat, Pittsburgh, PA 15213 USA
[3] Dept Vet Affairs Med Ctr, Neurol Serv, Pittsburgh, PA USA
关键词
muscular dystrophy; pharmacologic; therapy; DUCHENNE; BOYS; PREDNISONE; UTROPHIN; TRIAL; FRACTURES;
D O I
10.1097/WCO.0b013e328357f44c
中图分类号
R74 [神经病学与精神病学];
学科分类号
100204 [神经病学];
摘要
Purpose of review The study reviews recent advances in pharmacological management of muscular dystrophies. Similarities and differences among the pathophysiology of different forms of muscular dystrophy lead to a broad array of approaches to provide new treatments. Recent findings In this review, we include only those muscular dystrophies for which advances have been published in the past year. This represents the 'advancing edge' of a large body of research over more than 20 years. This runs the gamut of new discoveries in symptomatic management to mutation-specific strategies that attempt to correct the root cause of the disorder. Summary The field of pharmacological therapies for the muscular dystrophies continues to steadily advance. It is encouraging that research into new therapies is increasingly exploring pharmacological strategies with the potential to ameliorate disease pathology to a clinically significant degree.
引用
收藏
页码:604 / 608
页数:5
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