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
相关论文
共 50 条
[41]   Mucopolysaccharidoses and Other Lysosomal Storage Diseases [J].
Lampe, Christina ;
Bellettato, Cinzia Maria ;
Karabul, Nesrin ;
Scarpa, Maurizio .
RHEUMATIC DISEASE CLINICS OF NORTH AMERICA, 2013, 39 (02) :431-+
[42]   Disease Manifestations in Mucopolysaccharidoses and Their Impact on Anaesthesia-Related Complications-A Retrospective Analysis of 99 Patients [J].
Ammer, Luise Sophie ;
Dohrmann, Thorsten ;
Muschol, Nicole Maria ;
Lang, Annika ;
Breyer, Sandra Rafaela ;
Ozga, Ann-Kathrin ;
Petzoldt, Martin .
JOURNAL OF CLINICAL MEDICINE, 2021, 10 (16)
[43]   Pathogenesis of skeletal and connective tissue involvement in the mucopolysaccharidoses: glycosaminoglycan storage is merely the instigator [J].
Clarke, Lorne A. .
RHEUMATOLOGY, 2011, 50 :V13-V18
[44]   Musculoskeletal ultrasound in childhood [J].
Maurer, Kathrin .
EUROPEAN JOURNAL OF RADIOLOGY, 2014, 83 (09) :1529-1537
[45]   Musculoskeletal manifestations of mucopolysaccharidosis type VI and effects of enzyme replacement therapy [J].
Marucha, Jolanta ;
Jurecka, Agnieszka ;
Rozdzynska-Swiatkowska, Agnieszka ;
Tylki-Szymanska, Anna .
CENTRAL EUROPEAN JOURNAL OF MEDICINE, 2012, 7 (02) :154-162
[46]   Glaucoma in mucopolysaccharidoses [J].
Weijing Kong ;
Jing Zhang ;
Cheng Lu ;
Yingxue Ding ;
Yan Meng .
Orphanet Journal of Rare Diseases, 16
[47]   Overview of the mucopolysaccharidoses [J].
Muenzer, Joseph .
RHEUMATOLOGY, 2011, 50 :V4-V12
[48]   Glaucoma in mucopolysaccharidoses [J].
Kong, Weijing ;
Zhang, Jing ;
Lu, Cheng ;
Ding, Yingxue ;
Meng, Yan .
ORPHANET JOURNAL OF RARE DISEASES, 2021, 16 (01)
[49]   ENT and mucopolysaccharidoses [J].
Bianchi, Pier Marco ;
Gaini, Renato ;
Vitale, Silvano .
ITALIAN JOURNAL OF PEDIATRICS, 2018, 44
[50]   Progression of Cardiovascular Manifestations in Adults and Children With Mucopolysaccharidoses With and Without Enzyme Replacement Therapy [J].
Poswar, Fabiano de Oliveira ;
Santos, Hallana Souza ;
Santos, Angela Barreto Santiago ;
Berger, Solano Vinicius ;
Souza, Carolina Fischinger Moura de ;
Giugliani, Roberto ;
Baldo, Guilherme .
FRONTIERS IN CARDIOVASCULAR MEDICINE, 2022, 8