Speciali J G, Resende L A
Arq Neuropsiquiatr. 1984 Jun;42(2):166-70. doi: 10.1590/s0004-282x1984000200010.
The authors report a case of Parry-Romberg disease with predominantly facial left atrophy, seizures, amnesic aphasia, mental retardation, right hemiplegia and hemianesthesia, and cerebellar syndrome. The rarity of cerebellar atrophy (only one case thus far reported in the literature surveyed) is emphasized, as well as the correlation between the clinical abnormalities and the computerized axial tomography of the skull.
作者报告了一例主要表现为左侧面部萎缩、癫痫、遗忘性失语、智力发育迟缓、右侧偏瘫和偏身感觉障碍以及小脑综合征的Parry-Romberg病病例。强调了小脑萎缩的罕见性(在所查阅的文献中迄今仅报道过一例),以及临床异常与头颅计算机断层扫描之间的相关性。