儿童单基因糖尿病临床诊断与治疗专家共识

2019-07-25 中华医学会儿科学分会内分泌遗传代谢学组 中华儿科杂志.2019,57(7):508-514.

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

中文标题:

儿童单基因糖尿病临床诊断与治疗专家共识

发布日期:

2019-07-25

简要介绍:

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。

拓展指南:糖尿病相关指南:

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    2023-02-06 ms2000001024033712 来自广东省

    。。

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    2019-08-14 thm112988

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