DISSOLUTION OF RENAL CALCULI IN A CASE OF HEREDITARY FRUCTOSE INTOLERANCE AND RENAL TUBULAR ACIDOSIS
DISSOLUTION OF RENAL CALCULI IN A CASE OF HEREDITARY FRUCTOSE INTOLERANCE AND RENAL TUBULAR ACIDOSIS
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DOI：
10.1016/s0022-5347(17)63450-5
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发表时间：
1966-01-01
影响因子：
6.6
通讯作者：
VARNEY, JK
中科院分区：
文献类型：
--
作者：
HIGGINS, RB;VARNEY, JK
遗传性果糖不耐症是一种先天性代谢缺陷，由肝酶缺乏引起。1· 2葡萄糖的释放受到抑制，导致低血糖的临床表现通常与恶心、呕吐有关。腹泻、腹痛、嗜睡和昏迷。1-5虽然脑、肝和肾功能障碍已被证实，1，3-5，但既往未报道与肾小管酸中毒或肾钙质沉着症相关。本文报道了共存的遗传性果糖不耐症，肾小管性酸中毒和肾钙质沉着症，其中溶解的结石是achieved.CASE报告DFS，一个42岁的女人，被接纳到波特兰退伍军人管理局医院 * 在1963年11月，抱怨进行性全身无力点瘫痪。她入院时很无助。她的既往史显示终身性多剪和多尿;
Hereditary fructose intolerance is an inborn error of metabolism_ arising from a deficiency of a liver enzyme. 1• 2 Glucose release is inhibited with t, he resultant clinical manifestations of hypoglycemia often associated with nausea, vom. iting, diarrhea, abdominal pain, lethargy and coma. 1-5 Although cerebral, hepatic and renal dysfunctions have been documentecl, 1, 3-5 no previous association with renal tubular acidosis or nephrocalcinosis has been reported. This paper reports the coexistence of hereditary fructose intolerance, renal tubular acidosis and nephrocalcinosis wherein the dissolution of calculi was achieved.CASE REPORT DFS, a 42-year-old woman, was admitted to the Portland Veterans Administration Hospital* in November 1963, complaining of progressive generalized weakness to the point of paralysis. She was helpless on admission. Her past history revealed lifelong polyclipsia, and polyuria;