He Guohua, Zhang Hongwen, Cao Shanshan, Xiao Huijie, Yao Yong
Pediatrics, Peking University First Hospital, Beijing, China; Pediatrics, Foshan Maternal and Children's Hospital, Foshan, China.
Pediatrics, Peking University First Hospital, Beijing, China.
Intractable Rare Dis Res. 2016 Nov;5(4):297-300. doi: 10.5582/irdr.2016.01058.
Dent's disease is an X-linked recessive proximal tubular disorder that mostly affects male patients in childhood or early adult life. The condition is caused by mutations in the (Dent disease 1) or (Dent disease 2) genes located on chromosome Xp11.22 and Xq25, respectively. In most male patients, proteinuria is subnephrotic but may reach nephrotic levels. Here, we report the first case of Dent's disease complicated by nephrotic syndrome. Dent's disease should be considered in the differential diagnosis of nephrotic syndrome, and especially in male patients with early onset of nephrotic syndrome. A urinary α1-microglobulin/albumin ratio > 1 may provide the first clue to a tubulopathy.
丹特病是一种X连锁隐性近端肾小管疾病,主要影响儿童期或成年早期的男性患者。该病分别由位于Xp11.22和Xq25染色体上的CLCN5(丹特病1型)或OCRL(丹特病2型)基因突变引起。在大多数男性患者中,蛋白尿为亚肾病水平,但也可能达到肾病水平。在此,我们报告首例并发肾病综合征的丹特病病例。在肾病综合征的鉴别诊断中应考虑丹特病,尤其是肾病综合征早发的男性患者。尿α1-微球蛋白/白蛋白比值>1可能为肾小管疾病提供首个线索。