Reed U C, Rosemberg S, Diament A J, Scaff M, Canelas H M, Lefèvre A B
Arq Neuropsiquiatr. 1984 Sep;42(3):262-73. doi: 10.1590/s0004-282x1984000300010.
The authors report a case of Menkes' syndrome, probably the first one described in Brazil. The patient, a 15-month-old boy, showed pili torti, early progressive psychomotor deterioration and seizures. Serum levels of ceruloplasmin and copper were very low. Neuroradiological and roentgenological examinations revealed diffuse cerebral atrophy, arterial changes and bone abnormalities. At the post-mortem examination the more consistent findings were cerebral atrophy, neuronal loss in the thalamus and above all cerebellar cortical lesions. The disease has a sex-linked recessive inheritance and is believed to be caused by an inborn error of copper metabolism, perhaps subordinated to changes of proteins which carry copper to different tissues. The relevant literature in relation to the pathogenesis is reviewed.
作者报告了一例门克斯综合征病例,这可能是巴西描述的首例该病例。患者为一名15个月大的男孩,表现为扭曲发、早期进行性精神运动发育迟缓及癫痫发作。血清铜蓝蛋白和铜水平极低。神经放射学和X线检查显示弥漫性脑萎缩、动脉改变及骨骼异常。尸检时更一致的发现是脑萎缩、丘脑神经元丢失,尤其是小脑皮质病变。该疾病为X连锁隐性遗传,被认为是由铜代谢先天性缺陷引起的,可能与将铜转运至不同组织的蛋白质变化有关。本文对与发病机制相关的文献进行了综述。