Hadjichristou Christina, Christophidou-Anastasiadou Violetta, Bakopoulou Athina, Tanteles George A, Loizidou Maria A, Kyriacou Kyriacos, Hadjisavvas Andreas, Michalakis Konstantinos, Pissiotis Argyris, Koidis Petros
Int J Prosthodont. 2017 May/June;30(3):280–285. doi: 10.11607/ijp.5130. Epub 2017 Mar 20.
Oculo-dento-digital dysplasia (ODDD) is a congenital disorder manifesting with multiple phenotypic abnormalities involving the face, eyes, teeth, and limbs in addition to neurologic symptomatology. This report aims to present a female patient with ODDD who was referred due to extensive oral restorative needs. The presence of hypoplastic enamel triggered further evaluation. Characteristic facies with hypoplastic alae nasi and syndactyly offered greater insight into the phenotype of the syndrome. Clinical suspicion was confirmed by genetic sequencing revealing heterozygous mutation in GJA1. It is important to be aware of genetic disorders associated with characteristic dental malformations to offer appropriate counseling and treatment.
眼-牙-指发育不全(ODDD)是一种先天性疾病,除神经症状外,还表现为涉及面部、眼睛、牙齿和四肢的多种表型异常。本报告旨在介绍一名因广泛口腔修复需求前来就诊的ODDD女性患者。釉质发育不全的存在引发了进一步评估。具有鼻翼发育不全和并指畸形的特征性面容为该综合征的表型提供了更多线索。基因测序显示GJA1杂合突变,证实了临床怀疑。认识到与特征性牙齿畸形相关的遗传疾病,对于提供适当的咨询和治疗很重要。