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一名患有慢性复发性多神经病且对类固醇有反应的婴儿。

An infant with chronic, relapsing polyneuropathy responsive to steroids.

作者信息

Pasternak J F, Fulling K, Nelson J, Prensky A L

出版信息

Dev Med Child Neurol. 1982 Aug;24(4):504-24. doi: 10.1111/j.1469-8749.1982.tb13657.x.

DOI:10.1111/j.1469-8749.1982.tb13657.x
PMID:7117709
Abstract

A seven-week-old infant presented with an acute flaccid paraparesis. Her subsequent course was punctuated by numerous exacerbations, in association with minor intercurrent illness and remissions produced by corticosteroid treatment. Postmortem examination revealed a chronic inflammatory polyradiculopathy. She represents the youngest patient yet described with a chronic, relapsing, steroid-responsive polyneuropathy.

摘要

一名7周大的婴儿出现急性弛缓性双下肢轻瘫。其后续病程中多次病情加重,伴有轻微的并发疾病,且皮质类固醇治疗可使其缓解。尸检显示为慢性炎症性多发性神经根病。她是迄今所描述的患有慢性、复发性、类固醇反应性多发性神经病的最年幼患者。

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A Novel Cause of CIDP: Homozygous Hotspot Mutation, c.793 C > T in CASP8 Gene.慢性炎性脱髓鞘性多发性神经根神经病的一种新病因:CASP8基因纯合热点突变,c.793 C>T
J Clin Immunol. 2025 Sep 30;45(1):130. doi: 10.1007/s10875-025-01931-w.
2
Chronic inflammatory demyelinating polyneuropathy in two siblings.两名兄弟姐妹患慢性炎症性脱髓鞘性多发性神经病。
J Neurol Neurosurg Psychiatry. 1986 Feb;49(2):152-6. doi: 10.1136/jnnp.49.2.152.
3
Chronic inflammatory demyelinating polyneuropathy in childhood: ultrastructural features of peripheral nerve biopsies in four cases.
儿童慢性炎性脱髓鞘性多发性神经病:4例周围神经活检的超微结构特征
Eur J Pediatr. 1990 Jun;149(9):654-8. doi: 10.1007/BF02034757.
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Occurrence of active demyelinating lesions in children with hereditary motor and sensory neuropathy (HMSN) type I.遗传性运动和感觉神经病(HMSN)I型儿童中活动性脱髓鞘病变的发生情况。
Acta Neuropathol. 1992;84(4):433-6. doi: 10.1007/BF00227671.