遗传性肾炎为家族性疾病。临床特点为反复血尿、蛋白尿,进行性肾功能衰竭,部分病人合并耳聋与眼疾患。本病可能与遗传性代谢缺陷有关。现将作者所见3例报告如下。例1,男性,10岁。因浮肿、听力减退于1981年入院。尿蛋白(?),诊断为肾病综合征。入院后 Hereditary nephritis is a familial disease. Clinical features of repeated hematuria, proteinuria, progressive renal failure, some patients with deafness and eye diseases. The disease may be related to genetic metabolic defects. Now the author sees 3 cases reported as follows. Example 1, male, 10 years old. Due to edema, hearing loss admitted to hospital in 1981. Urinary protein (?), Diagnosed as nephrotic syndrome. After admission