New Developments in Juvenile Systemic and Localized Scleroderma

被引：13
|
作者：
Foeldvari, Ivan [1 ]
机构：
[1] Hamburger Zentrum Kinder & Jugendrheumatol, D-22081 Hamburg, Germany
来源：
RHEUMATIC DISEASE CLINICS OF NORTH AMERICA | 2013年 / 39卷 / 04期
关键词：
Juvenile localized scleroderma; Juvenile systemic sclerosis; Doppler ultrasonography; Biomarkers; STEM-CELL TRANSPLANTATION; INTERSTITIAL LUNG-DISEASE; 6-MINUTE WALK TEST; PULMONARY-HYPERTENSION; HEALTHY-CHILDREN; SKIN-DISEASE; INFRARED THERMOGRAPHY; SCLEROSIS; CHILDHOOD; TRIAL;
D O I：
10.1016/j.rdc.2013.05.003
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
Juvenile localized scleroderma (jLS) and juvenile systemic sclerosis (jSS) are both orphan diseases, with jLS around 10 times more frequent than jSS. In recent years the time gap between the appearance of symptoms and diagnosis has become significantly shorter. This review focuses on the new classifications of jSS and jLS, and on the developments and adaptations of the outcome measures for certain organ involvements whereby progress has been made regarding pediatric patients.
引用
收藏
页码：905 / +
页数：17
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