Distal Myopathies

被引:8
|
作者
Felice, Kevin J. [1 ,2 ,3 ]
机构
[1] Hosp Special Care, Charles H Kaman Fdn Neuromuscular, 2150 Corbin Ave, New Britain, CT 06053 USA
[2] Hosp Special Care, Muscular Dystrophy Assoc Care Ctr, 2150 Corbin Ave, New Britain, CT 06053 USA
[3] Univ Connecticut, Sch Med, Farmington, CT USA
关键词
Distal myopathy; Myofibrillar myopathy; Congenital myopathy; Muscular dystrophy; Genetic myopathy; MUSCULAR-DYSTROPHY FSHD; MUTATIONS; SKELETAL; GENE; DIAGNOSIS; DYSFERLIN; MYOSITIS; LINKAGE;
D O I
10.1016/j.ncl.2020.03.007
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The distal myopathies are a rare and heterogeneous group of neuromuscular disorders. Patients present with weakness of the hands, distal lower extremities, or both. Age of onset varies from early childhood to late adulthood. Most of the disorders causing distal myopathic weakness are genetically based. The list of genetic disorders associated with distal-onset weakness is ever-expanding and complicated by pronounced genetic heterogeneity, phenotypic variability, and complex multisystem involvement. There are no known effective disease-modifying treatments for the distal myopathies. Evaluation, symptomatic management, and periodic monitoring of patients in a multidisciplinary neuromuscular center are the mainstays of care. © 2020 Elsevier Inc.
引用
收藏
页码:637 / 659
页数:23
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