Creel D J, Summers C G, King R A
V.A. Medical Center, Salt Lake City, Utah.
Ophthalmic Paediatr Genet. 1990 Sep;11(3):193-200. doi: 10.3109/13816819009020979.
All mammals with hypopigmentation of the retinal pigment epithelium have abnormal visual systems. Albino mammals have been found to have: (1) reduced numbers of uncrossed optic fibers projecting to all visual centers, (2) disorganization of the pattern (lamination) of the dorsal lateral geniculate nuclei, and (3) disorganization of projections from the dorsal lateral geniculate nuclei to the visual cortex. The disorganization of central visual centers has catastrophic effects on stereovision and optokinetic nystagmus. Variable expression in oculocutaneous albinism suggests that affected individuals cannot always be identified by hypopigmentation, reduced visual acuity and nystagmus. Careful observation of foveal development in individuals even with normal vision is necessary to detect all persons with albinism. The scalp-recorded visually evoked potential designed to detect optic misrouting is the most reliable concomitant for determining albinism.
所有视网膜色素上皮色素减退的哺乳动物都有异常的视觉系统。已发现白化病哺乳动物有:(1)投射到所有视觉中枢的未交叉视神经纤维数量减少;(2)背外侧膝状核模式(分层)紊乱;(3)从背外侧膝状核到视觉皮层的投射紊乱。中枢视觉中枢的紊乱对视立体视觉和视动性眼球震颤有灾难性影响。眼皮肤白化病的可变表现表明,受影响的个体不能总是通过色素减退、视力下降和眼球震颤来识别。即使是视力正常的个体,也需要仔细观察其黄斑发育情况,以检测所有白化病患者。用于检测视神经错路的头皮记录视觉诱发电位是确定白化病最可靠的伴随指标。