Karch S B, Urich H
Dev Med Child Neurol. 1975 Aug;17(4):504-11. doi: 10.1111/j.1469-8749.1975.tb03502.x.
A case is reported of a boy who developed a severe polyneuropathy in early infancy and died of respiratory failure at the age of 18 months. Autopsy revealed almost total lack of myelin sheaths in the cranial, spinal and peripheral nerves. The defect involved the entire peripheral nervous system and was confined to it, central myelination being normal. It is suggested that this case is another example of the condition described by Lyon (1969) and by Kennedy et al. (1971) in which pathological observations were confined to biopsy material. In spite of some similarities between these cases and those of hypertrophic neuropathy reported by Déjerine and Sottas in 1893, they seem to form a distinct sub-group, possibly even a separate entity: infantile polyneuropathy with defective myelination.
报告了一例男婴,其在婴儿早期发生严重的多发性神经病,并于18个月时死于呼吸衰竭。尸检显示,在颅神经、脊神经和周围神经中几乎完全缺乏髓鞘。该缺陷累及整个周围神经系统且局限于此,中枢髓鞘形成正常。有人认为,该病例是Lyon(1969年)以及Kennedy等人(1971年)所描述病症的又一实例,在这些病例中,病理观察仅限于活检材料。尽管这些病例与1893年Déjerine和Sottas报道的肥厚性神经病病例存在一些相似之处,但它们似乎构成一个独特的亚组,甚至可能是一个独立的实体:髓鞘形成缺陷的婴儿多发性神经病。