Background: Anti-N-methyl-D-aspartate receptor immunoglobulin G antibodies directed against the GluN1 subunit are considered highly specific for anti-N-methyl-D-aspartate receptor encephalitis, a severe clinical syndrome characterized by seizures, psychiatric symptoms, orofacial dyskinesia and autonomic dysfunction. Case presentation: Here we report a 33 year old Caucasian male patient with clinically definite multiple sclerosis who was found to be positive for anti-N-methyl-D-aspartate receptor antibodies. Rituximab therapy was initiated. On the 18 months follow-up visit the patient was found to be clinically stable, without typical signs of anti-N-methyl-D-aspartate receptor encephalitis. Conclusion: Our findings add to the growing evidence for a possible association between anti-N-methyl-D-aspartate receptor encephalitis and demyelinating diseases.
CITATION STYLE
Waschbisch, A., Kallmünzer, B., Schwab, S., Gölitz, P., Vincent, A., Lee, D. H., & Linker, R. A. (2014). Demyelinating disease and anti-N-methyl-Daspartate receptor immunoglobulin G antibodies: A case report. BMC Research Notes, 7(1). https://doi.org/10.1186/1756-0500-7-948
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