Fukumori T, Tagawa T, Inui M
Department of Oral and Maxillofacial Surgery, Faculty of Medicine, Mie University, Japan.
Int J Oral Maxillofac Surg. 1993 Jun;22(3):139-44. doi: 10.1016/s0901-5027(05)80237-1.
A 23-year-old man with bilateral coronoid process hyperplasia and short stature is presented. These findings are characteristic features of trismus-pseudocampylodactyly syndrome. However, in this patient the pseudocampylodactyly component and family history were absent.
本文报告了一名23岁的男性,患有双侧冠状突增生和身材矮小。这些表现是牙关紧闭-假性弯曲指综合征的特征性表现。然而,该患者并无假性弯曲指这一症状,也无家族病史。