Shrestha J B, Shrestha G S, Joshi N, Karmacharya P C
B.P. Koirala Lions Centre for Ophthalmic Studies, Maharajgunj, Kathmandu.
Nepal J Ophthalmol. 2012 Jan-Jun;4(1):194-6. doi: 10.3126/nepjoph.v4i1.5877.
A case of congenital isolated coloboma of both the upper lids from just lateral to the lacrimal punctum up to the medial half, with symblepharon in the region of lower eyelid, was studied in a 7-year-old female child. She did not have any other associated anomalies. The birth and family histories were normal. The puncta were normal in position and well apposed to the globe. The closure of the lid coloboma was done by release of symblepharon along with direct closure of the defect, for the right eye first, and one month later, for the left eye.
对一名7岁女童进行了研究,该女童患有先天性双侧上睑裂孔,从泪点外侧直至内侧半侧,下睑区域有睑球粘连。她没有任何其他相关异常。出生史和家族史正常。泪点位置正常,与眼球贴合良好。首先对右眼进行睑裂孔闭合手术,通过松解睑球粘连并直接闭合缺损,一个月后对左眼进行同样手术。