Sari Ayça, Adigüzel Ufuk, Yeşilli Münevver, Aydin Ozlem, Oz Ozay
Mersin University School of Medicine, Mersin, Turkey.
J Cataract Refract Surg. 2008 Mar;34(3):523-4. doi: 10.1016/j.jcrs.2007.09.043.
We report 3 siblings from a nonconsanguineous white family with bilateral persistent pupillary membranes with dissimilar forms of severity. Two of the patients required no treatment; 1 was treated surgically for occlusion of the pupillary axis and moderate visual acuity decrease. Anterior segment examination was otherwise normal in the siblings. Although persistent pupillary membranes are usually sporadic, cases in which they are associated with other anterior chamber abnormalities might be inherited autosomal dominant. To our knowledge, this is the first report of a familial isolated persistent papillary membrane case with no other anterior chamber abnormality.
我们报告了一个非近亲结婚的白人家庭中的3名兄弟姐妹,他们患有双侧持续性瞳孔膜,严重程度各异。其中两名患者无需治疗;1名患者因瞳孔轴阻塞和视力中度下降接受了手术治疗。其他方面,这些兄弟姐妹的眼前节检查均正常。尽管持续性瞳孔膜通常是散发性的,但与其他前房异常相关的病例可能是常染色体显性遗传。据我们所知,这是首例无其他前房异常的家族性孤立性持续性瞳孔膜病例报告。