Appenzeller O, Kornfeld M, Snyder R
Arch Neurol. 1976 Nov;33(11):733-8. doi: 10.1001/archneur.1976.00500110001001.
Four Navajo children had a mutilating neuropathy with severe motor involvement. The disorder appears to be recessively inherited and is present from the earliest observable age. Manifestations include severe anesthesia, corneal ulceration, painless fractures, acral mutilation, and weakness. Mental function is normal. Sural nerves are practically devoid of myelinated fibers that show no evidence of regeneration. Unmyelinated axons show degenerative and regenerative morphologic and histometric features. Onion bulb formation is absent. We believe this neuropathy is a distinct clinical entity.
四名纳瓦霍儿童患有一种致残性神经病,伴有严重的运动功能受累。该疾病似乎为隐性遗传,在最早可观察到的年龄就已存在。表现包括严重的感觉缺失、角膜溃疡、无痛性骨折、肢体残毁和虚弱。智力功能正常。腓肠神经几乎没有有髓纤维,且无再生迹象。无髓轴突呈现出退行性和再生性的形态学及组织测量学特征。无葱皮样结构形成。我们认为这种神经病是一种独特的临床实体。