Cookies on this website

We use cookies to ensure that we give you the best experience on our website. If you click 'Accept all cookies' we'll assume that you are happy to receive all cookies and you won't see this message again. If you click 'Reject all non-essential cookies' only necessary cookies providing core functionality such as security, network management, and accessibility will be enabled. Click 'Find out more' for information on how to change your cookie settings.

A young girl with antibodies to the N-methyl-D-aspartate receptor presented with a clinical syndrome suggestive of dyskinetic encephalitis lethargica with neuropsychiatric features at presentation, movement disorder, mutism, sleep disorder, and seizures. Persistent lesions in the white matter and pons were observed in magnetic resonance imaging of the brain, findings that have not been described previously in N-methyl-D-aspartate receptor antibody encephalitis.

More information Original publication

DOI

10.1016/j.pediatrneurol.2010.05.004

Type

Journal article

Publication Date

2010-10-01T00:00:00+00:00

Volume

43

Pages

274 - 278

Total pages

4

Keywords

Autoantibodies, Brain, Child, Preschool, Electroencephalography, Encephalitis, Female, Humans, Magnetic Resonance Imaging, Receptors, N-Methyl-D-Aspartate, Seizures