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鉴于有关小儿尿酸盐肾病钙磷代谢的文献报道很少,为此,作者研究106例尿酸盐肾病患者,按年龄分组,将51例1～7岁患者分为第一组,55例8～14岁患者为第二组。用50得同龄健康儿童作为对照组。尿酸盐肾病的诊断标准:父母具有顽固的嘌呤代谢改变,存在尿酸素质、痛经、尿酸盐结石和其他尿酸病表现。早年(3～5岁)即表现肾脏疾病,尿液病理性改变包括白细胞尿、轻度血尿和蛋白尿、尿酸盐结石合并高水平的酸和氨成分,特殊的体质,动脉血压不稳定,胃肠功能失调,肌痛和关节痛,发作性呕吐,偏头痛等。
In view of the literature on calcium and phosphorus metabolism in children with urate nephropathy rarely reported, therefore, the study of 106 patients with urate nephropathy, grouped by age, 51 patients aged 1 to 7 years were divided into the first group, 55 cases of 8 ~ 14 years old patients for the second group. With 50 healthy children of the same age as a control group. Diagnostic criteria for urate nephropathy: Parents have stubborn purine metabolic changes, the presence of uric acid, dysmenorrhea, urate stones and other uric acid disease manifestations. Early years (3 to 5 years old) that the performance of kidney disease, pathological changes in urine, including leukocyturia, mild hematuria and proteinuria, uric acid stones with high levels of acid and ammonia components, special physique, arterial blood pressure instability, Gastrointestinal disorders, myalgia and arthralgia, paroxysmal vomiting, migraine and the like.