Abstract:IntroductionThe classic phenotype of anti-N-methyl-d-aspartate receptor (NMDA-R) encephalitis is a constellation of prodromal psychiatric symptoms, seizures, movement disorder and progressive autonomic dysfunction, frequently associated with ovarian teratoma. We describe four cases illustrating the expanding phenotype of NMDA-R encephalitis. We present two cases from two tertiary hospitals
Case 1 A 31 year old woman presented with focal onset seizures. She developed epilepsia partialis continua. CSF and serum … Show more
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