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儿童糖原累积病4例报告 被引量:2

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摘要 糖原累积病(glycogen storage disease,GSD)是一类由于先天性酶缺陷造成的糖原代谢障碍疾病,它可以出现机体能量代谢障碍和糖原异常堆积。多数属常染色体隐性遗传,少数属X连锁隐性遗传。少数属X连锁隐性遗传。Von Gierke在1929年首先描述了糖原累积病的临床表现和患者肝、肾组织中糖原堆积的病理改变。根据欧洲资料,其发病率为1/(2万-2.5万)。现将我院近年收治的4例糖原累积病报告如下。
出处 《临床儿科杂志》 CAS CSCD 北大核心 2009年第10期987-988,共2页 Journal of Clinical Pediatrics
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  • 1陈琳,郭玉璞,任海涛,赵燕环,关鸿志,管宇宙,彭斌,刘大为.少年起病的Ⅱ型糖原累积病五例临床病理研究[J].中华神经科杂志,2005,38(1):51-54. 被引量:15
  • 2谢新宝,朱启镕,王晓红,严秀峰,怀有为,俞蕙.儿童肝脏酶学异常328例病因分析[J].中国实用儿科杂志,2005,20(11):676-679. 被引量:5
  • 3杨天娇,王晓红,朱启镕.儿童肝糖原累积病的临床特点分析[J].中国临床医学,2007,14(2):209-210. 被引量:5
  • 4周华,方峰,徐三清,董永绥,李革.儿童代谢性肝沉积病肝组织病理和超微病理特征及其诊断意义[J].中国实用儿科杂志,2007,22(5):370-372. 被引量:10
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