Research Progress on Pathogenesis and Treatment of Juvenile Localized Scleroderma
Juvenile localized scleroderma (JLS) is a rare autoimmune disease in children. The lack of specificity in the early symptoms of JLS makes it easy to be misdiagnosed and missed, which leads to the continuous progression of the lesions, and even causes systemic malfunction and growth disorder. For ide...
Main Authors: | YANG Jingyi, XU Qianyue, YU Hong |
---|---|
Format: | Article |
Language: | zho |
Published: |
Editorial Office of Medical Journal of Peking Union Medical College Hospital
2022-01-01
|
Series: | Xiehe Yixue Zazhi |
Subjects: | |
Online Access: | https://xhyxzz.pumch.cn/en/article/doi/10.12290/xhyxzz.2021-0178 |
Similar Items
-
Juvenile Localized Scleroderma: A Very Rare Case
by: Nibedita Paul, et al.
Published: (2015-07-01) -
Baseline Description of the Juvenile Localized Scleroderma Subgroup From the Childhood Arthritis and Rheumatology Research Alliance Legacy Registry
by: Eveline Y. Wu, et al.
Published: (2019-04-01) -
The frequency of pulmonary hypertension in patients with juvenile scleroderma
by: Amra Adrovic, et al.
Published: (2015-08-01) -
Esophageal abnormalities in juvenile localized scleroderma: is it associated with other extracutaneous manifestations?
by: Clarissa C.M. Valões, et al. -
Juvenile localized scleroderma with port wine stain: Coincidental or possible common pathogenetic association
by: Seval Dogruk Kacar, et al.
Published: (2015-01-01)