Bejar J M, Ziegler D K
Arch Neurol. 1984 Aug;41(8):881-2. doi: 10.1001/archneur.1984.04050190087021.
A child, aged 24 months, incurred an episode of ataxic gait. Two months later, she had a recurrent episode of ataxic gait and bilateral blindness. Her symptoms were resolved with steroid therapy. A permanent visual deficit of 20/200 remained in the right eye. When she reached 16 years 10 months of age, she incurred the second episode of bilateral blindness. One month later, she had grand mal seizures. Her myelin basic protein level was elevated. Visual evoked responses were abnormal bilaterally. The combination of cerebellar, cortical, and eye symptoms, with a history of well-defined remissions, allowed the diagnosis of multiple sclerosis (MS) to be made. This is the youngest known patient with MS yet described, with the first attack occurring at 24 months of age.
一名24个月大的儿童出现了共济失调步态发作。两个月后,她再次出现共济失调步态发作并伴有双侧失明。她的症状通过类固醇治疗得到缓解。右眼仍存在20/200的永久性视力缺陷。当她16岁10个月大时,出现了第二次双侧失明发作。一个月后,她发生了大发作癫痫。她的髓鞘碱性蛋白水平升高。双侧视觉诱发电位异常。小脑、皮质和眼部症状的组合,以及明确的缓解病史,使得能够诊断为多发性硬化症(MS)。这是迄今所描述的已知患MS最年轻的患者,首次发作发生在24个月大时。