Dean J A, Jones J E, Vash B W
ASDC J Dent Child. 1986 Mar-Apr;53(2):131-4.
Oculodentodigital dysplasia is a rare autosomal dominant syndrome characterized by typical facies and certain anomalies of the eyes, dentition and digits. This report describes the case of a 2.5-year-old white male with oculodentodigital dysplasia and his comprehensive dental treatment. Aggressive treatment to maintain the integrity of the patient's primary dentition was provided. The characteristic physical and genetic findings of oculodentodigital dysplasia were also described.
眼牙指发育不全是一种罕见的常染色体显性综合征，其特征为典型面容以及眼睛、牙齿和手指的某些异常。本报告描述了一名患有眼牙指发育不全的2.5岁白人男性病例及其全面的牙科治疗情况。为维持患者乳牙列的完整性提供了积极治疗。还描述了眼牙指发育不全的特征性体格检查和基因检查结果。
