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范可尼综合征属肾小管性疾病范畴,为近曲管转运功能障碍造成的症候群。临床表现为生长发育迟缓、肢体疼痛、佝偻病、低血钾、酸中毒、旦白尿、糖尿及氨基酸尿等。兹将我院于1972年及1973年收治的2例儿童范可尼综合征报道如下:病例介绍[例1]杨××,男,11岁。自1～2岁起生长发育明显迟缓,且与同年龄小儿的差距逐年增大。伴肢体疼痛,行走不便,甚至需用拐杖勉强走200～300米。5岁起多饮多尿,每日饮水量达10～15磅,小便每日17～20次。食欲明显减退。曾于当地查尿常规:有旦白尿,少许红、白细胞及管型。诊断为“肾炎”、“垂体性尿崩症”、“垂体性侏
Fanconi’s syndrome is a category of renal tubular disease that is caused by a syndrome that is caused by a dysfunction of proximal tubule transport. Clinical manifestations of growth retardation, limb pain, rickets, hypokalemia, acidosis, proteinuria, diabetes and amino aciduria. We will be hospital in 1972 and 1973 admitted to 2 cases of children with Fanconi syndrome are reported as follows: Case introduction [Example 1] Yang × ×, male, 11 years old. Growth and development from the age of 1 to 2 significantly delayed, and the gap with the same age children increased year by year. Accompanied limb pain, walking inconvenience, and even need to walk barely walking 200 to 300 meters. 5-year-old to drink more urine, daily drinking water up to 10 to 15 pounds, urine 17 to 20 times a day. Appetite decreased significantly. Urine routine inspection at the local: a white urine, a little red, white blood cells and tube. Diagnosed as “nephritis”, “pituitary diabetes insipidus”, "pituitary dwarf