Gabreëls-Festen A A, Joosten E M, Gabreëls F J, Stegeman D F, Vos A J, Busch H F
Institute of Neurology, University Hospital, Nijmegen, The Netherlands.
Brain. 1990 Dec;113 ( Pt 6):1629-43. doi: 10.1093/brain/113.6.1629.
Six patients (5 index cases and 1 sib) with a congenital motor and sensory neuropathy are described. The clinical, genetic and electrophysiological features resembled Dejerine-Sottas disease or hereditary motor and sensory neuropathy (HMSN) type III. Sural nerve biopsy of 5 patients revealed segmental demyelination and remyelination with hypertrophic changes, although onion bulbs were not as ubiquitous as in classical HMSN type III. A striking discriminating feature from HMSN type III was an abundance of focal myelin thickenings (tomacula) present in nearly all teased fibres. Possible pathogenic implications are discussed. These cases corroborate the heterogeneity of congenital motor and sensory neuropathies.
本文描述了6例患有先天性运动和感觉神经病变的患者(5例索引病例和1例同胞患者)。其临床、遗传和电生理特征类似于德热里纳 - 索塔斯病或遗传性运动和感觉神经病变(HMSN)III型。5例患者的腓肠神经活检显示节段性脱髓鞘和再髓鞘化伴肥厚性改变,尽管洋葱球并不像经典的HMSN III型那样普遍存在。与HMSN III型的一个显著区别特征是几乎所有分离的神经纤维中都存在大量局灶性髓鞘增厚(髓鞘瘤)。文中讨论了可能的致病意义。这些病例证实了先天性运动和感觉神经病变的异质性。