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作 者:徐晓丽 廖涌 蒲丹岚 杨刚毅[1] 李伶[4] XU Xiaoli;LIAO Yong;PU Danlan;YANG Gangyi;LI Ling(Department of Endocrinology,The Second Affiliated Hospital of Chongqing Medical University,Chongqing 400010,China;Department of Endocrinology,Armed Police Chongqing General Hospital,Chongqing 400061,China;Department of Endocrinology,Yubei District People′s Hospital of Chongqing,Chongqing 401120,China;Teaching and Research Section of Clinical Biochemistry,College of Laboratory,Chongqing Medical University,Key Laboratory of Clinical Laboratory Diagnostics Founded by Ministry of Education,Chongqing 400016,China)
机构地区:[1]重庆医科大学附属第二医院内分泌科,重庆400010 [2]武警重庆总队医院内分泌科,重庆400061 [3]重庆市渝北区人民医院内分泌科,重庆401120 [4]重庆医科大学检验医学院临床生化教研室/教育部临床检验诊断学重点实验室,重庆400016
出 处:《现代医药卫生》2023年第18期3152-3156,共5页Journal of Modern Medicine & Health
基 金:重庆市自然科学基金项目(CSTB2022NSCQ-MSX1271)。
摘 要:家族性白蛋白异常性高甲状腺素血症(FDH)是临床上甲状腺功能正常的高甲状腺素血症的常见原因之一,易被误诊为甲状腺毒症。若进一步给予不必要的相关治疗,可能导致一系列的后续疾病出现。因此加强对FDH的认识十分必要。该文就其发病机制、检测手段、鉴别诊断等方面进行综述,为认识FDH提供临床参考。Familial dysalbuminemic hyperthyroxinemia(FDH)is one of the common causes of hyperthyroidism with normal thyroid function in clinic,which is easily misdiagnosed as thyrotoxicosis.If further treatment is given unnecessarily,it may lead to a series of subsequent diseases.Therefore,it is necessary to strengthen the understanding of FDH.This article reviewed its pathogenesis,detection methods,differential diagnosis and other aspects to provide further clinical reference for FDH.
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