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据不完全统计,我院于1983—1984年共收治抗D佝偻病4例,现将资料较完整之1例低血磷抗维生素D佝偻病报道如下。罗宽宁,男,6岁,病历号17826。以双下肢“X”畸形5个月于1984年3月25日住院。患儿1周岁前与同龄儿无异,2岁开始迈步,3岁才能独立行走。行路腿软,尤以上坡明显,出牙晚,牙色黄易碎。5月前发现患儿双下肢呈明显“X”形,走路摇摆。智力好,食欲可,二便正常。曾于同年2月按抗D佝偻病在门诊治疗(服鱼肝油)糖钙片,用过维生素D_3,剂量不详)约40~+天,无效。患儿系1胎1产,早产1个月,新生儿期曾患肺炎,硬肿。父母非近亲婚配。无遗传病史。家中无类似患者。体检:T37.2℃,P103次/分,R24次/分,
According to incomplete statistics, our hospital in 1983-1984 received a total of 4 cases of anti-D rickets, now a more complete data of 1 case of hypophosphatemic anti-vitamin D rickets reported below. Luo Kuanning, male, 6 years old, medical record number 17826. To double lower extremity “X” deformity 5 months in March 25, 1984 hospitalization. 1 year old children with their children the same age, 2 years old began to move, 3 years old to walk independently. Leg legs soft, especially in the obvious slope, teething, tooth yellow fragile. May found that children with lower extremities was significantly “X” -shaped, walking swing. Good intelligence, appetite, two will be normal. In February the same year by anti-D rickets in the outpatient treatment (serving cod liver oil) calcium tablets, used vitamin D_3, dose unknown) about 40 ~ + days, invalid. Children with 1 fetus 1 birth, 1 month premature birth, neonatal pneumonia, had swollen. Parents non-relatives marriage. No history of genetic disease. No similar patients at home. Physical examination: T37.2 ℃, P103 times / min, R24 times / min,