Kinsey J A, Streeten B W
Am J Ophthalmol. 1977 Feb;83(2):261-6. doi: 10.1016/0002-9394(77)90625-0.
An 8-month-old infant boy with median facial cleft syndrome had eyelid coloboma, symblepharon, and a cytic mass in the left upper eyelid. The mass proved to be an ectatic cornea containing a large cystic lens. Maldevelopment of the entire anterior segment of the eye was also present, although the posterior globe was well formed. We postulate that an area of localized abnormal mesodermal differentiation and fusion at the 17- to 20-mm stage of development served as a common mechanism for all the defects noted.
一名患有面正中裂综合征的8个月男婴有眼睑缺损、睑球粘连和左上眼睑囊性肿物。该肿物被证实是一个扩张的角膜,其中包含一个大的囊性晶状体。尽管眼球后部结构正常,但整个眼前段均发育不良。我们推测,在发育的17至20毫米阶段,局部中胚层分化和融合异常区域是所有上述缺陷的共同发病机制。