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Azathioprine therapy in a case of pediatric multiple sclerosis that was seropositive for MOG-IgG
Journal article   Peer reviewed

Azathioprine therapy in a case of pediatric multiple sclerosis that was seropositive for MOG-IgG

Y. Zhou, Q. Huang, T. Lu, X. Sun, L. Fang, Z. Lu, X. Hu, A. Kermode and W. Qiu
Journal of Clinical Neuroscience, Vol.38, pp.71-73
2017
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Abstract

There is a lack of evidence for treatment of pediatric multiple sclerosis (PedMS). Treatment using azathioprine for PedMS has not been reported. A 10-year-old boy with multiple sclerosis who was seropositive for antibodies against myelin oligodendrocyte glycoprotein (MOG)-IgG was treated with azathioprine plus oral methylprednisolone. The patient showed clinical and magnetic resonance imaging stability, with MOG-IgG seroconversion. There were no major side effects over a 5-year period. Azathioprine may be a treatment option, particularly in poor medical resource areas, for pediatric patients with multiple sclerosis who are seropositive for MOG-IgG.

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Collaboration types
Domestic collaboration
International collaboration
Citation topics
1 Clinical & Life Sciences
1.203 Neuromuscular Disorders
1.203.147 Multiple Sclerosis
Web Of Science research areas
Clinical Neurology
Neurosciences
ESI research areas
Neuroscience & Behavior
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