Tachi N, Ishikawa Y, Minami R
Brain Dev. 1984;6(6):560-5. doi: 10.1016/s0387-7604(84)80101-1.
The clinical features and findings in biopsied sural nerves of two cases of congenital hypomyelination neuropathy were reported. Case 1 had slightly retarded motor milestones without evidence of respiratory distress during the neonatal period. Case 2 had difficulty in swallowing and respiration after birth and severely delayed motor milestones. The sural nerve, on light microscopy, revealed reduced density of myelinated fibers in the two cases. Electron microscopy disclosed hypomyelination without evidence of active demyelination or axonal changes in the two cases. Onion-bulbs were composed of concentric whorls of Schwann cell process surrounding particularly small myelinated fibers in case 1 and of concentric lamellae, mainly consisting of two parallel layers of basement membrane, in case 2. Congenital hypomyelination neuropathy shows variability of clinical features such as in our two cases. We suspected that there was gradation of severity both in clinical expression and in the disorder of Schwann cells.
报告了两例先天性髓鞘形成不足性神经病患者活检腓肠神经的临床特征和发现。病例1运动发育里程碑略有延迟,新生儿期无呼吸窘迫迹象。病例2出生后有吞咽和呼吸困难,运动发育里程碑严重延迟。光镜下,两例患者的腓肠神经显示有髓纤维密度降低。电镜显示两例均为髓鞘形成不足,无活动性脱髓鞘或轴突改变的证据。病例1中洋葱球由围绕特别小的有髓纤维的施万细胞突起同心环组成,病例2中洋葱球由同心板层组成,主要由两层平行的基底膜组成。先天性髓鞘形成不足性神经病表现出临床特征的变异性,如我们的两例患者。我们怀疑在临床表型和施万细胞疾病方面都存在严重程度的分级。