Creel D J, Bendel C M, Wiesner G L, Wirtschafter J D, Arthur D C, King R A
N Engl J Med. 1986 Jun 19;314(25):1606-9. doi: 10.1056/NEJM198606193142503.
Patients with oculocutaneous or ocular albinism have misrouting of optic fibers, with fibers from 20 degrees or more of the temporal retina crossing at the chiasm instead of projecting to the ipsilateral hemisphere. Misrouting can result in strabismus and nystagmus. Because patients with the Prader-Willi syndrome may also have hypopigmentation and strabismus, we wondered whether they too might have misrouting of optic fibers. We therefore studied six patients with Prader-Willi syndrome selected for a history of strabismus, using pattern-onset visually evoked potentials with binocular and monocular stimulation to look for evidence of misrouted retinal-ganglion fibers. Four had hypopigmentation, and three of these four had abnormal evoked potentials indistinguishable from those recorded in human albinos. The two with normal pigmentation had normal responses. These findings indicate that patients with Prader-Willi syndrome who have hypopigmentation have a brain abnormality characterized by misrouting of retinal-ganglion fibers at the optic chiasm--a finding previously reported only in forms of albinism.
患有眼皮肤白化病或眼白化病的患者存在视神经纤维错路,来自颞侧视网膜20度或更大范围的纤维在视交叉处交叉,而不是投射到同侧半球。错路可导致斜视和眼球震颤。由于普拉德-威利综合征患者也可能有色素减退和斜视,我们想知道他们是否也存在视神经纤维错路。因此,我们研究了六名因有斜视病史而入选的普拉德-威利综合征患者,使用双眼和单眼刺激的图形起始视觉诱发电位来寻找视网膜神经节纤维错路的证据。其中四名有色素减退,这四名中的三名有异常诱发电位,与在人类白化病患者中记录的诱发电位无法区分。另外两名色素正常的患者反应正常。这些发现表明,患有色素减退的普拉德-威利综合征患者存在一种脑部异常,其特征是视交叉处视网膜神经节纤维错路——这一发现此前仅在白化病的某些类型中报道过。