Murphy Rinki
Department of Medicine, Faculty of Medical and Health Sciences, University of Auckland, Auckland, New Zealand.
Obstet Med. 2015 Sep;8(3):114-20. doi: 10.1177/1753495X15590713. Epub 2015 Jun 29.
Monogenic diabetes is frequently mistakenly diagnosed as either type 1 or type 2 diabetes, yet accounts for approximately 1-2% of diabetes. Identifying monogenic forms of diabetes has practical implications for specific therapy, screening of family members and genetic counselling. The most common forms of monogenic diabetes are due to glucokinase (GCK), hepatocyte nuclear factor (HNF)-1A and HNF-4A, HNF-1B, m.3243A>G gene defects. Practical aspects of their recognition, diagnosis and management are outlined, particularly as they relate to pregnancy. This knowledge is important for all physicians managing diabetes in pregnancy, given this is a time when previously unrecognised monogenic diabetes may be uncovered with careful attention to atypical features of diabetes misclassified as type 1, type 2, or gestational diabetes.
单基因糖尿病常被误诊为1型或2型糖尿病,但约占糖尿病患者的1%-2%。识别单基因糖尿病类型对特定治疗、家庭成员筛查及遗传咨询具有实际意义。最常见的单基因糖尿病类型是由葡萄糖激酶(GCK)、肝细胞核因子(HNF)-1A、HNF-4A、HNF-1B、m.3243A>G基因缺陷引起的。本文概述了它们在识别、诊断和管理方面的实际情况,尤其是与妊娠相关的情况。鉴于在孕期仔细关注被误诊为1型、2型或妊娠期糖尿病的糖尿病非典型特征时,可能发现之前未被识别的单基因糖尿病,这些知识对所有管理孕期糖尿病的医生都很重要。