Systemic juvenile idiopathic arthritis complicated with PSTPIP1 gene variant: A case report

Yutong Gao, Yuqing Chen
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Abstract

Objective: Systemic Juvenile Idiopathic Arthritis (SJIA) is a subtype of childhood rheumatoid arthritis, with the main clinical manifestations of high fever, recurrent rash, and arthritis. At present, it is generally believed that it is caused by the interaction of gene and environmental factors and has complex genetic characteristics. We report a case of a 1-year and 4-month SJIA patient with heterozygous mutation in PSTPIP1, and we studied the literature on this gene and related autoinfl ammatory diseases.
系统性青少年特发性关节炎合并PSTPIP1基因变异1例
目的:系统性少年特发性关节炎(Systemic Juvenile Idiopathic Arthritis, SJIA)是儿童类风湿关节炎的一种亚型,主要临床表现为高热、反复发疹、关节炎。目前普遍认为它是由基因和环境因素共同作用引起的,具有复杂的遗传特征。我们报告1例1岁零4个月的SJIA患者PSTPIP1杂合突变,并对该基因及相关自身炎症性疾病的文献进行了研究。
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