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从“肝肾同源”论治特纳综合征

Differentiation and treatment of Turner syndrome from the perspective of “liver and kidney homogeny”

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【作者】 邓湘玲王琼张知新

【Author】 DENG Xiangling;WANG Qiong;Zhang Zhixin;Beijing University of Chinese Medicine;China-Japan Friendship Hospital;

【通讯作者】 张知新;

【机构】 北京中医药大学中日友好医院

【摘要】 特纳综合征由于遗传物质丢失,导致身材矮小,性腺发育不良,五脏六腑发育不足,这与中医学“先天不足”“肝肾不足”相吻合。在肝肾同源理论的视角下分析特纳综合征的发病机制及肝肾不足对特纳综合征的多方面影响,临证从肝郁脾虚证、肝血亏虚证、肝肾亏虚证辨治有一定疗效。

【Abstract】 Due to the loss of genetic materials,patients with a Turner syndrome are characterized by short statures,gonadal dysplasia,and underdevelopment of zang-fu viscera,which are consistent with the pattern “congenital insufficiency” and the pattern of “insufficiency of the liver and kidney” in traditional Chinese medicine.Therefore,this paper attempts to analyze the pathogenesis of a Turner syndrome from the perspective of the liver-kidney homogeny theory,and discuss the multi-faceted effects of the liver-kidney insufficiency syndrome on the disease,proposing to differentiate and treat it from the three aspects in clinic:syndrome of stagnation of liver qi and spleen deficiency,syndrome of deficiency of liver blood,and syndrome of deficiency of both the liver and kidney.

【基金】 国家自然科学基金项目(41571376)
  • 【文献出处】 吉林中医药 ,Jilin Journal of Chinese Medicine , 编辑部邮箱 ,2022年07期
  • 【分类号】R259
  • 【下载频次】157
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