Ruhin B, Martinot V, Lafforgue P, Catteau B, Manouvrier-Hanu S, Ferri J
Department of Oral and Maxillofacial Surgery, Roger Salengro University Hospital, Boulevard du Professeur Leclercq, 59037 Lille Cedex, France.
Cleft Palate Craniofac J. 2001 Sep;38(5):504-18. doi: 10.1597/1545-1569_2001_038_0504_pedrso_2.0.co_2.
To review the possible craniomaxillofacial deformative consequences associated with ectodermal dysplasias and embryonic malformations, which include dental ageneses.
Oral and Maxillofacial Surgery Department, University Hospital, Lille, France.
Sixteen patients (seven boys and nine girls, aged 4 to 34 years) with pure ectodermal dysplasia (no ectodermal dysplasia syndromes).
All patients had a clinical examination. Seven (two boys and five girls, aged 4 to 25 years) had undergone plaster casts and radiographic and Delaire's cephalometric studies before being treated.
All patients had tooth ageneses (from hypodontia to anodontia), associated with cutaneous dyshidrosis and hair and nail dystrophy. Most of them had a short face, with an unusual facial concavity, a maxillary retrusion, and a relative mandibular protrusion. MANAGEMENT RESULTS AND DISCUSSION: Depending on their ages and their orthopedic abnormalities, patients underwent either dental or prosthodontic, orthodontic, orthopedic, orthognathic, or implant treatment. So as not to interfere with the growth pattern, we preferred to reserve implant and orthognathic surgery for full-grown cases.
Oral and maxillofacial surgeons must undertake a comprehensive approach to these patients to improve their dental, masticatory, growing, and orthognathic conditions.
回顾与外胚层发育不全及胚胎畸形(包括牙胚缺失)相关的可能的颅颌面畸形后果。
法国里尔大学医院口腔颌面外科。
16例单纯性外胚层发育不全患者(7名男性和9名女性,年龄4至34岁)(无外胚层发育不全综合征)。
所有患者均接受临床检查。其中7例(2名男性和5名女性,年龄4至25岁)在接受治疗前已进行石膏模型、影像学及德莱尔头影测量研究。
所有患者均有牙胚缺失(从牙量不足到无牙症),伴有皮肤出汗障碍及毛发和指甲营养不良。他们中的大多数面部较短,面部有异常凹陷、上颌后缩及相对的下颌前突。治疗结果与讨论:根据患者年龄及骨骼异常情况,患者接受了牙科或修复、正畸、正颌、矫形或种植治疗。为不干扰生长模式,我们倾向于为成年病例保留种植和正颌手术。
口腔颌面外科医生必须对这些患者采取综合治疗方法,以改善他们的牙齿、咀嚼、生长及正颌状况。