Alaygut Demet, Torun-Bayram Meral, Soylu Alper, Kasap Belde, Türkmen Mehmet, Kavukçu Salih
Division of Pediatric Nephrology, Department of Pediatrics, Dokuz Eylül University Faculty of Medicine, İzmir, Turkey.
Turk J Pediatr. 2013 Nov-Dec;55(6):637-40.
Chronic kidney disease (CKD) is a life-long condition associated with substantial morbidity and premature death due to complications from a progressive decrease in kidney function. Especially in children, early diagnosis and detection of the etiologic factors are important to improve their health outcomes. Familial juvenile hyperuricemic nephropathy (FJHN) is a rare autosomal-dominant disorder characterized by hyperuricemia with renal uric acid under-excretion and CKD. Genetic studies have revealed mutations in the uromodulin (UMOD) gene. Highlighting the importance of CKD in children, a 14-year-old girl with the rare diagnosis of FJHN is reported herein.
慢性肾脏病(CKD)是一种终身疾病,由于肾功能逐渐下降引发的并发症,常伴有严重的发病率和过早死亡。特别是在儿童中,早期诊断和病因检测对于改善他们的健康状况至关重要。家族性青少年高尿酸血症肾病(FJHN)是一种罕见的常染色体显性疾病,其特征为高尿酸血症伴肾脏尿酸排泄不足及慢性肾脏病。基因研究已揭示尿调节蛋白(UMOD)基因存在突变。本文报道了一名罕见诊断为FJHN的14岁女孩,凸显了儿童慢性肾脏病的重要性。