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作 者:张琳滋 孔庆辉 ZHANG Linzi;KONG Qinghui(Grade 2020 Graduate,Shandong University of Traditional Chinese Medicine,Shandong Province,Jinan 250355,China;Department of Hepatobiliary Diseases,Weihai Hospital of Traditional Chinese Medicine,Shandong Province,Weihai 264200,China)
机构地区:[1]山东中医药大学,山东济南250355 [2]威海市中医院肝胆病科,山东威海264200
出 处:《中国中医药现代远程教育》2024年第4期70-72,共3页Chinese Medicine Modern Distance Education of China
摘 要:肝豆状核变性(Hepatolenticular degeneration,HLD)是遗传性铜代谢障碍的常染色体隐性遗传疾病,其主要特点为肝脏和神经系统受累。此文报道孔庆辉教授曾收治的肝豆状核变性合并肝硬化腹水出现慢性肝衰竭病案1例,对其临床资料进行分析和整理,希冀能提高同行对本病的认识。Hepatolenticular degeneration(HLD) is an autosomal recessive genetic disorder of hereditary copper metabolism,and it is mainly characterized by involvement of the liver and nervous system.The clinical manifestations of patients are different.Ascites due to cirrhosis is a serious clinical complication in patients with HLD,and it faces many difficulties in treatment.This paper reported a case of chronic liver failure caused by HLD complicated with ascites of cirrhosis treated by Professor Kong Qinghui.The clinical data of this case were analyzed and sorted out,hoping to improve the understanding of the colleagues of this disease.
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