原发性肾性葡萄糖尿是一种肾小管葡萄糖回吸收的遗传性缺陷,一般分为A型和B型。作者报告了一例具有肾小管葡萄糖回吸收完全丧失的男该,并建议称之为O型肾性葡萄糖尿。 患者男性15岁。主诉为持续的多饮、多尿、夜尿和贪食。身高159cm,体重60kg、查体无异常发现。血清钾、钠、氯、钙、磷、碳酸氢盐、肌酐、尿素氮、蛋白和免疫球蛋白、肝和肌肉的诸酶以及各内分泌腺的激素均正常。患者每天从尿中排出葡 Primary renal glucoseuria is a genetic defect of renal tubular glucose absorption, generally divided into A and B type. The authors report a case of male with complete loss of tubular glucose recovery and recommended o-type renal glucoseuria. The patient is 15 years old. The chief complaint was persistent drinking, polyuria, nocturia and bulimia. Height 159cm, weight 60kg, no abnormal findings. Serum potassium, sodium, chlorine, calcium, phosphorus, bicarbonate, creatinine, urea nitrogen, protein and immunoglobulin, liver and muscle enzymes and hormones of the endocrine glands are normal. The patient excretes glucose from the urine every day