Sekhar H K, Sachs M, Siverls V C
Ann Otol Rhinol Laryngol. 1987 May-Jun;96(3 Pt 1):309-14. doi: 10.1177/000348948709600314.
We report two cases of Hanhart's syndrome. The first patient was a male who died in the neonatal period, and whose temporal bones were removed, processed, and histologically examined; the findings are presented in this article. The second case concerns a living patient with the typical characteristics of the syndrome. An attempt is made to show that a gross first and second branchial arch anomaly exists in this syndrome and not just the micrognathia that is obvious to the onlooker. Possible causes and classifications of facial dysmorphia are discussed.
我们报告两例汉哈特综合征病例。首例患者为一名男性，死于新生儿期，其颞骨被摘除、处理并进行了组织学检查；本文展示了检查结果。第二例为一名患有该综合征典型特征的在世患者。本文试图表明，该综合征存在明显的第一和第二鳃弓大畸形，而非仅存在旁观者易见的小颌畸形。文中还讨论了面部畸形的可能病因及分类。
