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特发性范科尼综合征的代谢异常:两名患者的碳水化合物代谢研究

Metabolic abnormalities in the idiopathic Fanconi syndrome: studies of carbohydrate metabolism in two patients.

作者信息

Chesney R W, Kaplan B S, Teitel D, Colle E, McInnes R R, Goldman H, Scriver C R

出版信息

Pediatrics. 1981 Jan;67(1):113-8.

PMID:7017570
Abstract

Two patients with idiopathic Fanconi syndrome and glucose intolerance were studied from a metabolic perspective. They had fasting hyperglycemia, massive glucosuria, insulinopenia, ketosis, and elevated serum free fatty acids. There was a markedly blunted insulin secretory response to glucagon, tolbutamide, glucose, and arginine. One patient had the findings of diabetic retinopathy and a sensory neuropathy. Neither patient could convert galactose to glucose, but they did not have galactosemia. As a result of these studies, and previous reports in which similar changes were noted, we conclude that diabetes mellitus may occur in patients who have had idiopathic Fanconi syndrome for many years.

摘要

从代谢角度对两名患有特发性范科尼综合征和葡萄糖不耐受的患者进行了研究。他们有空腹高血糖、大量糖尿、胰岛素缺乏、酮症以及血清游离脂肪酸升高。对胰高血糖素、甲苯磺丁脲、葡萄糖和精氨酸的胰岛素分泌反应明显迟钝。一名患者有糖尿病视网膜病变和感觉神经病变的表现。两名患者均不能将半乳糖转化为葡萄糖,但他们没有半乳糖血症。基于这些研究以及之前有类似变化的报告,我们得出结论,多年患有特发性范科尼综合征的患者可能会发生糖尿病。

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