| 마이엘린 희소돌기아교세포 당단백질(Myelin Oligodendrocyte Glycoprotein) 자가항체 양성뇌척수염 환자들의 임상적 다양성에 대한 증례보고 2예 |
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김성현, 곽동원, 오지영, 최교민 |
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건국대학교병원 신경과 |
| Case Reports of Clinical Variability in Myelin Oligodendrocyte Glycoprotein (MOG ) Encephalom yelitis Patients |
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Sung Hyun Kim, Dong Won Kwack, Jeeyoung Oh, Kyomin Choi |
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Department of Neurology, Konkuk University Medical Center, Seoul, Korea |
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| Abstract |
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"Most experts now consider myelin oligodendrocyte glycoprotein (MOG) antibody positive encepha- lomyelitis as a disease entity immunopathogenetically distinct from multiple sclerosis and neuro-myelitis optica spectrum disorder (NMOSD). MOG-encephalomyelitis patients usually present withrecurrent optic neuritis or limb paralysis due to myelitis, but also behavioral change, seizures, or en- cephalopathies are often the first manifestations in these patients. Herein, we report two cases ofMOG-antibody encephalomyelitis who presented with atypical symptoms that included aggressivebehavior, multiple cranial neuropathies, and seizures.Journal of Multiple Sclerosis 10(2):32-35, 2019 |
| Key Words:
Myelin-oligodendrocyte glycoprotein, Encephalomyelitis, Magnetic resonance imaging |
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