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遗传性肾炎(Alport综合症)临床特点为血尿、进行性慢性肾功能衰竭及神经性耳聋。现报道我区一家系三例患者如下: 例1 男,12岁,壮族。反复浮肿,进行性苍白4年,加重一周,于1988年2月22日入院。体重23kg,血压14.3/10.4kPa,发育营养差,慢性重度贫血病容,颜面浮肿,尿红细胞(+)、蛋白(++)。Bcr1414μmol/L,BUN63mmol/L,CO_2CP10mmol/L,胆固醇4.5mmol/L,血浆总蛋白59g/L;
Hereditary nephritis (Alport syndrome) clinical features of hematuria, progressive chronic renal failure and neurological deafness. It is reported that a family of three patients in our district are as follows: 1 male, 12 years old, Zhuang. Repeated edema, progressive pale 4 years, an increase of one week, in February 22, 1988 admission. Weight 23kg, blood pressure 14.3 / 10.4kPa, poor nutrition, chronic severe anemia, facial edema, urine red blood cells (+), protein (++). Bcr1414μmol / L, BUN63mmol / L, CO_2CP10mmol / L, cholesterol 4.5mmol / L, total plasma protein 59g / L;