The clinical features of hereditary nephrotic syndrome caused by NPHS 2 mutation in two pediatric patients
10.3969/j.issn.1000-3606.2016.12.013
- VernacularTitle:NPHS2基因突变致遗传性肾病综合征患儿临床特点
- Author:
Jieyuan CUI
;
Hongwen ZHANG
- Keywords:
hereditary nephrotic syndrome;
NPHS2 gene;
clinical feature;
child
- From:
Journal of Clinical Pediatrics
2016;34(12):933-935
- CountryChina
- Language:Chinese
-
Abstract:
Objective To explore the clinical features of steroid resistant nephrotic syndrome caused by NPHS2 gene mutation. Methods The clinical data of two pediatric patients with steroid resistant nephrotic syndrome were retrospectively analyzed. The pertinent literatures were reviewed. Results Both patients were male with onset age at 2 and 3 years old. The clinical features were heavy proteinuria, hypoalbuminemia, and hypercholesterolemia, which met the diagnostic criteria of nephrotic syndrome. Renal pathology found one patient with focal segmental glomerulosclerosis, and other with minimal-change. Both of them suffered from recurrent inguinal hernioplasty and one was accompanied with hypoplasia of left testis. Gene detection verified a NPHS2 gene mutation. Both of them were hormone resistant at the beginning of onset and later hormone combined with different kinds of immunosuppressive therapy was still ineffective. Both of them entered the end-stage of renal disease 3 years after onset. Conclusions For male pediatric patients with steroid resistant nephrotic syndrome, combined with non-renal manifestations such as multiple hernia or testicular abnormalities, the possibility of the hereditary nephrotic syndrome caused by NPHS2 mutations should be considered.
