Shpak A A, Aznaurian I É, Balasanian V O, Tavtilova D A
Vestn Oftalmol. 2012 Jul-Aug;128(4):66-9.
Two clinical cases of children with foveal hypoplasia and high visual acuity examined using optical coherence tomography are presented. Genetic examination found oculocutaneous albinism type 1 in one patient. Potential causes and functional value of foveal hypoplasia are discussed.
本文介绍了两例使用光学相干断层扫描检查的患有黄斑发育不全且视力良好的儿童临床病例。基因检查发现其中一名患者患有1型眼皮肤白化病。文中讨论了黄斑发育不全的潜在病因和功能价值。