Schmidt H, Kuhnle U
Dr. von Haunerschen Kinderspital, Universitäts-Kinderklinik München.
Klin Padiatr. 1993 Mar-Apr;205(2):116-8. doi: 10.1055/s-2007-1025209.
We report on a 2-year old boy with the characteristic features of Di George syndrome. The diagnosis was confirmed by history, biochemical, immunologic and radiologic findings. After physical exercise he developed an unilateral epiphysiolysis capitis femoris, rarely seen in this age and not known to be a complication of hypoparathyroidism.
我们报告了一名患有迪乔治综合征典型特征的2岁男孩。通过病史、生化、免疫和放射学检查结果确诊。体育锻炼后,他出现了单侧股骨头骨骺溶解,这在该年龄段很少见,且未知是甲状旁腺功能减退的并发症。