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一名新生儿的先天性髓鞘形成不足性神经病

Congenital hypomyelination neuropathy in a newborn.

作者信息

Hakamada S, Kumagai T, Hara K, Miyazaki S, Miyazaki K, Watanabe K

出版信息

Neuropediatrics. 1983 Aug;14(3):182-3. doi: 10.1055/s-2008-1059575.

Abstract

A case of infantile neuropathy with signs of respiratory distress and impaired abdominal movements from the neonatal period was reported. Muscle biopsy revealed type II fiber predominance and atrophy, and the sural nerve biopsy demonstrated the absence of myelin in almost all of the axons. Onion bulb formation or myelin debris was not observed. The features of myelin deficit without active myelin breakdown and onion bulb formation, and the finding of muscle pathology, indicating the absence of spinal muscular atrophy, suggested that the case under study was identical to that of hypomyelination neuropathy.

摘要

报告了1例自新生儿期起即有呼吸窘迫体征和腹部运动障碍的婴儿神经病病例。肌肉活检显示Ⅱ型纤维占优势和萎缩,腓肠神经活检显示几乎所有轴突均无髓鞘。未观察到洋葱球形成或髓鞘碎片。无活动性髓鞘破坏和洋葱球形成的髓鞘缺乏特征以及肌肉病理学发现(表明不存在脊髓性肌萎缩)提示,所研究的病例与低髓鞘性神经病相同。

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