Singh K K, Kumar R, Prakash J, Krishna A
Department of Pediatrics, Indira Gandhi Institute of Medical Sciences, Patna, Bihar, India.
Department of Nephrology, Indira Gandhi Institute of Medical Sciences, Patna, Bihar, India.
Indian J Nephrol. 2015 Sep-Oct;25(5):300-2. doi: 10.4103/0971-4065.151765.
Bardet-Biedl syndrome (BBS) is a rare autosomal recessive disorder characterized by postaxial polydactyly, retinitis pigmentosa, central obesity, mental retardation, hypogonadism, and renal involvement. Renal involvement in various forms has been seen in BBS. Cases with nephrotic range proteinuria not responding to steroid have been described in this syndrome. Here we report a case of BBS who presented with nephrotic range proteinuria. The biopsy findings were suggestive of minimal change disease. The child responded well to steroid therapy and remains in remission.
巴德-比埃尔综合征(BBS)是一种罕见的常染色体隐性疾病,其特征为轴后多指畸形、色素性视网膜炎、中心性肥胖、智力发育迟缓、性腺功能减退和肾脏受累。BBS可见多种形式的肾脏受累。该综合征中曾描述过对类固醇无反应的肾病范围蛋白尿病例。在此,我们报告一例表现为肾病范围蛋白尿的BBS病例。活检结果提示为微小病变病。该患儿对类固醇治疗反应良好,目前仍处于缓解期。