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遗传性运动和感觉神经病I型的常染色体隐性形式。

Autosomal recessive form of hereditary motor and sensory neuropathy type I.

作者信息

Gabreëls-Festen A A, Gabreëls F J, Jennekens F G, Joosten E M, Janssen-van Kempen T W

机构信息

Institute of Neurology, University Hospital Nijmegen, The Netherlands.

出版信息

Neurology. 1992 Sep;42(9):1755-61. doi: 10.1212/wnl.42.9.1755.

Abstract

We studied pathologic changes in sural nerve biopsies from four patients with probable autosomal recessive (AR) hereditary motor and sensory neuropathy (HMSN) type I with a median motor nerve conduction velocity greater than 10 m/sec, comparing them with the pathologic features in autosomal dominant (AD) HMSN type I. The four recessive and two sporadic cases showed segmental demyelination. However, the classic onion bulbs of concentric Schwann cell processes, which occur in AD type I, were rare; many axons, also of a smaller size, were surrounded by onion bulbs of basal laminae. Schwann cells of the myelinated and unmyelinated types were involved in these onion bulb formations. Patients with HMSN type I who have many basal lamina onion bulbs should be considered as having AR inheritance.

摘要

我们研究了4例可能为常染色体隐性(AR)遗传性运动感觉神经病(HMSN)I型、运动神经传导速度中位数大于10米/秒的患者腓肠神经活检的病理变化,并将其与常染色体显性(AD)HMSN I型的病理特征进行比较。4例隐性病例和2例散发病例均显示节段性脱髓鞘。然而,AD I型中出现的由同心许旺细胞突起构成的典型洋葱球很少见;许多轴突,其直径也较小,被基底膜洋葱球所包绕。有髓和无髓型许旺细胞均参与了这些洋葱球的形成。具有许多基底膜洋葱球的HMSN I型患者应被视为具有AR遗传方式。

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