Myelin oligodendrocyte glycoprotein-antibody (MOG-IgG) associated disease with centrally located long spinal cord lesion in a 14-month old child.

IF 2.6 Q2 CLINICAL NEUROLOGY Journal of Central Nervous System Disease Pub Date : 2020-09-09 eCollection Date: 2020-01-01 DOI:10.1177/1179573520955008
Mohamad Syafeeq Faeez Md Noh
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引用次数: 2

Abstract

Myelin oligodendrocyte glycoprotein-antibodies (MOG-IgG) are associated with acquired inflammatory demyelinating syndromes, seen predominantly in children and young adults. The overlapping clinical and radiological features of the heterogenous spectrum of demyelinating central nervous system (CNS) diseases makes the detection of MOG-IgG antibodies important for prognosis and treatment decisions. Herein, we describe the occurrence of MOG-IgG associated disease presenting as acute disseminated encephalomyelitis (ADEM), with spinal MRI findings of centrally located long cord lesion in a 14-month old child.

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髓鞘少突胶质细胞糖蛋白抗体(MOG-IgG)相关疾病伴中央定位长脊髓病变1例14月龄儿童
髓鞘少突胶质细胞糖蛋白抗体(MOG-IgG)与获得性炎症性脱髓鞘综合征相关,主要见于儿童和年轻人。脱髓鞘中枢神经系统(CNS)疾病异质性谱的重叠临床和影像学特征使得MOG-IgG抗体的检测对预后和治疗决策很重要。在此,我们描述了一名14个月大的儿童发生的MOG-IgG相关疾病,表现为急性播散性脑脊髓炎(ADEM),脊柱MRI显示为中央位置的长脊髓病变。
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CiteScore
6.90
自引率
0.00%
发文量
39
审稿时长
8 weeks
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