Peña-Cardelles Juan-Francisco, Domínguez-Medina David A, Cano-Durán Jorge A, Ortega-Concepción Daniel, Cebrián José-Luis
DDS, Oral Medicine Postgraduate in Complutense University of Madrid. Oral and Maxillofacial Surgery Service, Alcorcon Southern Hospital.
MD, Oral and Maxillofacial Surgery Service, Alcorcon Southern Hospital.
J Clin Exp Dent. 2019 Mar 1;11(3):e290-e295. doi: 10.4317/jced.55543. eCollection 2019 Mar.
Ellis-van Creveld syndrome (EVC) or chondroectodermal dysplasia is an autosomal recessive disorder, characterized by dwarfism, polydactyly, hypoplastic fingernails and congenital heart defects, finding in most of the cases orofacial anomalies. We describe a clinical case of a 9 year old male patient diagnosed with EVC who visited our Maxillofacial private consultation at Alcorcon Southern Hospital, presenting typical oral manifestations such as dental agenesis, delayed eruption, hypoplasia of the enamel, dental dysmorphism, taurodontism and supernumerary teeth. EVC syndrome is a rare disease and requires a multidisciplinary approach. Oral features are constant and requires the jointly performance of Odontologist and Maxillofacial surgeon aiming to get an appropriate treatment sequence surgery-orthodontics in order to achieve a suitable functional result to improve the quality of life of these patients. Ellis-Van creveld syndrome, chondroectodermal dysplasia, oral manifestations, craniofacial manifestations.
埃利斯-范克里维尔德综合征(EVC)或软骨外胚层发育不良是一种常染色体隐性疾病,其特征为侏儒症、多指(趾)畸形、指甲发育不全和先天性心脏缺陷,多数病例还伴有口面部异常。我们描述了一例9岁男性患者的临床病例,该患者被诊断为EVC,前来我们位于阿尔科孔南部医院(Alcorcon Southern Hospital)的颌面私人诊所就诊,表现出典型的口腔症状,如牙齿缺失、萌出延迟、釉质发育不全、牙齿形态异常、牛牙症和多生牙。EVC综合征是一种罕见疾病,需要多学科方法进行治疗。口腔特征较为固定,需要牙科医生和颌面外科医生共同协作,制定合适的治疗顺序,即先手术再正畸,以获得理想的功能效果,提高这些患者的生活质量。埃利斯-范克里维尔德综合征、软骨外胚层发育不良、口腔表现、颅面部表现