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儿童单基因糖尿病临床诊断与治疗专家共识 被引量:17

Expert consensus on the diagnosis and management of monogenic diabetes in children and adolescents
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摘要 随着对糖尿病发病机制认识的深入,以单基因糖尿病为主的特殊类型糖尿病正日益引起人们的关注。单基因糖尿病变异占儿童糖尿病的1%~6%,但大多数单基因糖尿病在早期易被误诊。分子遗传学检测是确诊单基因糖尿病的首要方法,为进一步规范中国儿童单基因糖尿病的诊断、分型、治疗、随访、并发症和合并症的评估及防治,由中华医学会儿科学分会内分泌遗传代谢学组组织专家讨论,并参考国内外的最新指南,同时结合国内外流行病学调查、临床研究成果,制订本共识。
作者 中华医学会儿科学分会内分泌遗传代谢学组 傅君芬 罗小平 The Subspecidlty Group of Endocrinological Hereditary and Metabolic Disease the Society of Pediatrics Chinese Medical Association;Fu Junfen;Luo Xiaoping(Department of Endocrinology, the Children's Hospital of Zhejiang University School of Medicine, Hangzhou 310052, China;Department of Pediatrics, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, China)
出处 《中华儿科杂志》 CAS CSCD 北大核心 2019年第7期508-514,共7页 Chinese Journal of Pediatrics
基金 国家自然科学基金(81570759) 十三五国家重点研发计划(2016YFC1305300) 2018国家卫生计生委科学研究基金-浙江省医药卫生重大科技计划重大项目(WKJ-ZJ-1804) 浙江省医学重点学科(创新学科)(11-CX24) 中央高校基本科研业务费专项资金(2017xzzx001-01).
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