患有NPHS2突变的儿童患有性综合征
Ross Tollaksen1, Randall D Craver2, Ihor V Yosypiv1
1Departments of Pediatrics, Section of Pediatric Nephrology, Tulane University Health Sciences Center, New Orleans, LA, USA.
概括
早期对儿童的类固醇耐药性性综合征 (SRNS) 的基因检测至关重要. 识别NPHS2基因变异可以避免不必要的免疫抑制,并指导这种病的适当治疗.
科学领域:
- 儿科脏病学 儿科脏病学
- 医学遗传学 医学遗传学
背景情况:
- 类固醇耐药性性综合征 (SRNS) 影响30%的儿科性综合征 (NS) 病例,往往进展到末期病 (ESKD).
- 大约30%的儿科SRNS病例与podocyte相关基因的突变有关,突出显示了遗传学的作用.
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