Musculoskeletal manifestations of mucopolysaccharidoses

被引:63
作者
Morishita, Kimberly [1 ]
Petty, Ross E. [1 ]
机构
[1] British Columbia Childrens Hosp, Div Rheumatol, Dept Pediat, Vancouver, BC V6H 3V4, Canada
关键词
Mucopolysaccharidoses; Contractures; Musculoskeletal; MPS; Juvenile idiopathic arthritis; Rheumatology; Inflammation; Dysostosis multiplex; CARPAL-TUNNEL-SYNDROME; LYSOSOMAL STORAGE DISORDERS; JUVENILE IDIOPATHIC ARTHRITIS; HURLER-SCHEIE-SYNDROME; JOINT DISEASE; TRIGGER FINGERS; COMPLICATIONS; CHILDREN; BONE; TRANSPLANTATION;
D O I
10.1093/rheumatology/ker397
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The mucopolysaccharidoses (MPSs) are a heterogeneous group of inherited metabolic disorders caused by enzyme deficiencies that lead to progressive lysosomal storage of glycosaminoglycans. Musculoskeletal manifestations are common across all forms of MPS and are often apparent early in the disease course. Diagnostic delays occur frequently in these patients, especially those with more attenuated forms of disease. Treatments for many types of MPS are now available; however, they are most effective if started early before the development of irreversible damage. Some manifestations such as stiffness and joint contractures may mimic other conditions such as inflammatory arthritis, which may cause further delays. Rheumatologists and other specialists should be aware of the musculoskeletal manifestations of MPS so that diagnostic delays can be avoided and appropriate management initiated.
引用
收藏
页码:V19 / V25
页数:7
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