Abstract
Anti-N-methyl D-aspartate receptor (anti-NMDAR) encephalitis is the most common and best described of the autoimmune encephalitis syndromes associated with neuronal cell surface or synaptic autoantibodies. It is typically characterised by a progressive clinical course involving confusion, psychosis, seizures, dysautonomia and altered consciousness and has increasingly been a diagnostic consideration for clinicians given greater awareness of its serious nature and potential response to immunosuppressive therapy.
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