Schuller M G, Barnett M L, Strassburger K, Friedman D L, Sonnenberg E M
Oral Surg Oral Med Oral Pathol. 1986 Apr;61(4):418-21. doi: 10.1016/0030-4220(86)90431-7.
A case of oculodentodigital dysplasia in a 35-year-old man is reported. The diagnosis was based on the characteristic facies, microcornea, and dental dysplasia. Digital findings, although consistent with previous reports, were somewhat atypical, with almost complete aplasia of the right foot present. Although the patient appeared to be mentally retarded, it is not clear whether this can be considered a component of the syndrome or merely a coincidental finding.
报告了一名35岁男性患眼齿指发育异常的病例。诊断基于特征性面容、小角膜和牙齿发育异常。手指表现虽然与先前报道一致,但有些不典型,右脚几乎完全发育不全。尽管患者似乎有智力障碍,但尚不清楚这是该综合征的一部分还是仅仅是一个偶然发现。