Virani Zaheer A, Rajput Prashant, Vora Hepal, Shah Bharat V
Department of Nephrology, Institute of Renal Sciences, Global Hospital Parel-12, Mumbai, Maharashtra, India.
Indian J Nephrol. 2021 Sep-Oct;31(5):485-487. doi: 10.4103/ijn.IJN_172_20. Epub 2021 Feb 20.
A 37 years old female presented with asymptomatic nephrotic range proteinuria due to focal segmental glomerulosclerosis (FSGS). She was treated with steroids and mycophenolate mofetil to which there was no response and progressed to advanced chronic kidney disease. When her brother who was being evaluated as a potential donor, for renal transplant, was found to have proteinuria and a genetic study for the steroid-resistant nephrotic syndrome was done. This revealed mutation in the gene. It is then that a diagnosis of nail-patella syndrome (NPS) was made. She underwent a successful renal transplant with her father as a donor and is doing well.
一名37岁女性因局灶节段性肾小球硬化(FSGS)出现无症状性肾病范围蛋白尿。她接受了类固醇和霉酚酸酯治疗,但无反应,病情进展为晚期慢性肾脏病。当她作为肾移植潜在供体接受评估的哥哥被发现有蛋白尿时,针对类固醇抵抗性肾病综合征进行了基因研究。这揭示了该基因的突变。随后确诊为指甲-髌骨综合征(NPS)。她以父亲为供体成功接受了肾移植,目前情况良好。