Wiley C A, Love S, Skoglund R R, Lampert P W
Acta Neuropathol. 1987;72(4):369-76. doi: 10.1007/BF00687269.
A caucasian male with a history of mental retardation and intractable epilepsy since birth, developed progressive wasting and weakness of skeletal muscles, leading to death at 4 years of age. A biopsy of gastrocnemius muscle at 2 years of age revealed severe neurogenic atrophy. Sural nerve biopsies at 2 and 3 years showed progressive atrophy and loss of large myelinated nerve fibers with a paucity of neurofilaments in remaining nerve fibers. Postmortem immunohistochemical and ultrastructural examination showed that neurons were markedly distended by phosphorylated neurofilaments. Whereas large lower motor neurons were most severely involved, dorsal root ganglia and neurons in the cerebral cortex and deep gray nuclei were also affected. It is suggested that this disease is caused by a disorder of neurofilament phosphorylation and transport.
一名自出生就患有智力发育迟缓及顽固性癫痫的白种男性,逐渐出现骨骼肌进行性消瘦和无力,4岁时死亡。2岁时腓肠肌活检显示严重的神经源性萎缩。2岁和3岁时的腓肠神经活检显示大的有髓神经纤维进行性萎缩和丧失,剩余神经纤维中神经丝缺乏。尸检免疫组化和超微结构检查显示神经元被磷酸化神经丝显著扩张。虽然大型下运动神经元受累最严重,但背根神经节以及大脑皮层和深部灰质核团中的神经元也受到影响。提示该疾病是由神经丝磷酸化和运输障碍引起的。