Recurrent ataxia and dysarthria in myelin oligodendrocyte glycoprotein antibody-associated disorder

被引：0

作者：

Chakraborty, Uddalak ^{[1
]}

Ghosh, Shrestha ^{[2
]}

Dana, Amlan Kusum ^{[1
]}

Chandra, Atanu ^{[2
]}

机构：

[1] Inst Postgrad Med Educ & Res, Neurol, Bangur Inst Neurol, Kolkata, W Bengal, India

[2] RG Kar Med Coll & Hosp, Internal Med, Kolkata, W Bengal, India

来源：

BMJ CASE REPORTS | 2021年 / 14卷 / 11期

关键词：

neurology; neuroimaging; immunology; DIAGNOSIS; CHILDREN; DISEASE;

D O I：

10.1136/bcr-2021-245341

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

The spectrum of central nervous system demyelinating disorders is vast and heterogeneous and, often, with overlapping clinical presentations. Misdiagnosis might occur in some cases with serious therapeutic repercussions. However, introduction of several new biomarkers such as aquaporin-4 IgG and myelin oligodendrocyte glycoprotein IgG has made distinction between diseases such as multiple sclerosis and myelin oligodendrocyte glycoprotein antibody-associated disorder easier. Here, we report a case of a 15-year-old male patient with subacute multifocal neurological presentation without encephalopathy, eventually diagnosed as myelin oligodendrocyte glycoprotein antibody-associated disorder.

引用

页数：4

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