Taşar F, Bulut E, Tümer C, Saysel M, Muhtarogullari M
Department of Oral Surgery, Faculty of Dentistry, University of Hacettepe, Ankara, Turkey.
Aust Dent J. 1995 Dec;40(6):352-6. doi: 10.1111/j.1834-7819.1995.tb04831.x.
A 29-year-old Caucasian woman who presented with short stature and multiple unerupted supernumerary teeth is described. Radiological investigations of her cranial and skeletal abnormalities revealed cleidocranial dysplasia. Because of the advanced age of the patient and contraindication for orthodontic treatment, only surgical and prosthetic treatment were performed. The characteristics and treatments of this rare autosomal dominant disorder are discussed.
本文描述了一位29岁的白种女性,她身材矮小且有多个未萌出的额外牙齿。对其颅骨和骨骼异常进行的放射学检查显示为锁骨颅骨发育不全。由于患者年龄较大且正畸治疗存在禁忌证,仅进行了手术和修复治疗。本文讨论了这种罕见的常染色体显性疾病的特征和治疗方法。