Kornfeld M, Synder R D, MacGee J, Appenzeller O
Arch Neurol. 1975 Feb;32(2):103-7. doi: 10.1001/archneur.1975.00490440053008.
Clinical, light microscopical, ultrastructural, and biochemical studies were done on nerve and muscle biopsy specimens from five patients with the oculo-cerebral-renal syndrome of Lowe. Four patients were American Indians, a racial group in whom this disease has not previously been recognized. The hypotonia, areflexia, and diffuse atrophy of muscles are associated with slowed motor nerve conduction velocities, and the morphologic changes in sensory nerves are attributed to a "dying-back" phenomenon probably resulting from an unknown metabolic derangement.
对5例患有洛氏眼脑肾综合征患者的神经和肌肉活检标本进行了临床、光学显微镜、超微结构和生化研究。4例患者为美洲印第安人,此前该种族尚未发现有这种疾病。肌肉的张力减退、反射消失和弥漫性萎缩与运动神经传导速度减慢有关,感觉神经的形态学变化归因于可能由未知代谢紊乱导致的“逆行性变性”现象。