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Update on Juvenile Spondyloarthritis
被引:25
|作者:
Ramanathan, Anusha
[1
]
Srinivasalu, Hemalatha
[2
]
Colbert, Robert A.
[3
]
机构:
[1] Childrens Hosp Los Angeles, Keck Sch Med USC, Div Rheumatol, Los Angeles, CA 90027 USA
[2] George Washington Univ, Childrens Natl Med Ctr, Div Rheumatol, Washington, DC 20010 USA
[3] Natl Inst Arthrit Musculoskeletal & Skin Dis NIAM, Pediat Translat Res Branch, NIH, Bethesda, MD 20892 USA
关键词:
Juvenile spondyloarthritis;
Enthesitis-related arthritis;
Juvenile psoriatic arthritis;
HLA-B27;
Axial spondyloarthritis;
ENTHESITIS-RELATED ARTHRITIS;
ACTIVE ANKYLOSING-SPONDYLITIS;
DISTAL INTERPHALANGEAL JOINT;
ANTITUMOR NECROSIS FACTOR;
SOCIETY CLASSIFICATION CRITERIA;
MAJOR CLINICAL-RESPONSE;
IDIOPATHIC ARTHRITIS;
PSORIATIC-ARTHRITIS;
RADIOGRAPHIC PROGRESSION;
AXIAL SPONDYLOARTHRITIS;
D O I:
10.1016/j.rdc.2013.06.002
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
Spondyloarthritis (SpA) encompasses a group of disorders linked by overlapping clinical manifestations and genetic predisposition. Newer classification systems developed for adults with SpA focus on identifying individuals with axial or predominantly peripheral involvement. All forms of SpA can begin during childhood, and can be considered on a continuum with adult disease. Nevertheless, there are important differences in presentation and outcome that depend on age at onset. This article highlights these differences, what has been learned about genetics and pathogenesis of SpA, and important unmet needs for future studies.
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页码:767 / +
页数:23
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