Shield J P H
Bristol Royal Hospital for Children, Department of Child Health, Bristol, UK.
Horm Res. 2007;68 Suppl 5:32-6. doi: 10.1159/000110471. Epub 2007 Dec 10.
Nine distinct genetic conditions have been identified in the last 12 years causing neonatal diabetes mellitus through failure of normal pancreatic development, islet cell dysfunction or beta-cell destruction. This review will focus on the three conditions about which our understanding of the pathology - and in some cases the treatment options - has greatly increased: transient neonatal diabetes mellitus, permanent neonatal diabetes due to 'channelopathies' and immune dysregulation, polyendocrinopathy, enteropathy X-linked syndrome.
Effective treatment of neonatal diabetes requires thorough understanding of the disease processes underlying this highly variable condition. As our knowledge of pancreatic development and physiology expands, so, too, do the treatment options for some patients.
在过去12年中,已鉴定出9种不同的遗传病症,这些病症通过正常胰腺发育失败、胰岛细胞功能障碍或β细胞破坏导致新生儿糖尿病。本综述将聚焦于三种病症,我们对其病理学(在某些情况下还包括治疗选择)的理解有了极大的提升:短暂性新生儿糖尿病、由“离子通道病”和免疫失调、多内分泌腺病、肠病X连锁综合征引起的永久性新生儿糖尿病。
有效治疗新生儿糖尿病需要深入了解这种高度可变病症背后的疾病过程。随着我们对胰腺发育和生理学知识的扩展,一些患者的治疗选择也在增加。