遗传性肾炎又称Alport综合征,是一种少见的家族性肾脏疾病.我科近来收治1例,报告如下: 患者茹某,男,20岁.因尿蛋白2年余,伴恶心,呕吐3个月于1988年4月23日入院.患者12岁起出现听力下降,并逐渐加重至耳聋,伴面色苍白,头昏,乏力,视力逐渐减退.两年前在当地医院检查,发现尿中有蛋白,红细胞及管型,并持续存在,按 Hereditary nephritis, also known as Alport syndrome, is a rare familial renal disease.Our department recently admitted in 1 case, the report is as follows: patient Rumou, male, 20 years old, due to urinary protein more than 2 years, with nausea and vomiting Month in April 23, 1988. Patients with hearing loss since the age of 12, and gradually increased to deafness, with pale, dizziness, fatigue, vision diminished. Two years ago at the local hospital examination and found that urine Proteins, erythrocytes and tube type, and persist, press