Streeten B W, Karpik A G, Spitzer K H
Arch Ophthalmol. 1983 Apr;101(4):616-22. doi: 10.1001/archopht.1983.01040010616019.
A 16-year-old girl with bilateral congenital posterior keratoconus of the localized type had corneal transplantation performed on one eye. Around the scarred central corneal cone there was a ring of Descemet's membrane with large knob-like excrescences. A small anterior subcapsular cataract was also present in this eye. The pattern of corneal scarring, as seen by electron microscopy, suggested an iridocorneal or iridocorneolenticular adhesion present at the 8- to 20-mm embryonic stage. Associated systemic defects, which could be dated to the same period, were median facial clefting and severe genitourinary abnormalities. Several external features, such as short stature, abnormal gait, broad nose, and upward displacement of the lateral canthi, were similar to those in the Haney-Falls syndrome of familial posterior keratoconus. No appreciable chromosomal abnormalities were found.
一名16岁双侧先天性局限性后圆锥角膜女孩接受了单眼角膜移植手术。在瘢痕化的中央角膜圆锥周围有一圈带有大的瘤状赘生物的Descemet膜。该眼还存在一个小的前囊下白内障。电子显微镜下所见的角膜瘢痕模式提示在胚胎8至20毫米阶段存在虹膜角膜或虹膜角膜晶状体粘连。可追溯到同一时期的相关全身缺陷为面部正中裂和严重的泌尿生殖系统异常。一些外部特征,如身材矮小、步态异常、宽鼻和外眦上移,与家族性后圆锥角膜的哈尼 - 福尔斯综合征相似。未发现明显的染色体异常。