Nagashima K, Yagi H, Kuroume T
Department of Pediatrics, Gunma University School of Medicine, Japan.
Clin Genet. 1993 Feb;43(2):98-100. doi: 10.1111/j.1399-0004.1993.tb04458.x.
We report a girl with Johanson-Blizzard syndrome complicated by diabetes mellitus. She presented several characteristic malformations, such as aplasia of the alae nasi, deafness, dwarfism, absence of permanent teeth and malabsorption caused by disturbance of pancreatic exocrine function. At 11 years of age, glycosuria was detected at a routine outpatient examination. Repeated oral glucose tests showed a slowly progressive decline of insulin secretion and elevated blood glucose levels. The responsive secretion of insulin to glucagon or arginine loading was also low. The blood level of HbAlc was elevated over 9%. Based on these findings, insulin therapy was started when the patient was 13 years old. Our case suggests that diabetes mellitus might be considered as one of complications of Johanson-Blizzard syndrome.
我们报告了一名患有乔汉森-布莱兹德综合征并伴有糖尿病的女孩。她出现了多种特征性畸形,如鼻翼发育不全、耳聋、侏儒症、恒牙缺失以及胰腺外分泌功能紊乱导致的吸收不良。11岁时,在一次常规门诊检查中发现了糖尿。多次口服葡萄糖测试显示胰岛素分泌缓慢进行性下降且血糖水平升高。胰岛素对胰高血糖素或精氨酸负荷的反应性分泌也较低。糖化血红蛋白(HbAlc)的血液水平升高超过9%。基于这些发现,患者13岁时开始胰岛素治疗。我们的病例表明,糖尿病可能被视为乔汉森-布莱兹德综合征的并发症之一。