Clinical outcome in an infant with anti-NMDA receptor encephalitis: Case report and literature review

Anti N-methyl-D-aspartate receptor (NMDAR) encephalitis is an autoimmune disease that often presents with various neurological and neuropsychiatric symptoms. Although most reported cases occur in children, only a limited number of studies on children are available. The subject of this case report is...

Full description

Saved in:
Bibliographic Details
Published inInternational journal of neuroscience Vol. 133; no. 11; pp. 1 - 1251
Main Authors Cavusoglu, Dilek, Ozer Gokaslan, Cigdem, Olgac Dundar, Nihal
Format Journal Article
LanguageEnglish
Published England 02.11.2023
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:Anti N-methyl-D-aspartate receptor (NMDAR) encephalitis is an autoimmune disease that often presents with various neurological and neuropsychiatric symptoms. Although most reported cases occur in children, only a limited number of studies on children are available. The subject of this case report is an 8-month-old female who presented with fever, vomiting, and seizure. She was diagnosed with encephalitis and treated with acyclovir. After 21 days, she showed irritability, seizure, orolingual-facial dyskinesias, choreodystonic movements, hemiparesis, dysphagia, strabismus, lack of interest in light and objects. Clinical signs, neuroimaging findings, and serum analysis of anti-NMDAR antibodies confirmed the diagnosis of anti-NMDAR encephalitis. After the first line of treatment, she showed full recovery. We update the infants with anti-NMDAR encephalitis in the literature. Clinical outcomes suggest that patients with anti-NMDAR encephalitis are mostly poor in the infants, excluding our case. We propose that early and appropriate treatments are critical for timely diagnosis and rapid improvement.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:0020-7454
1563-5279
1543-5245
DOI:10.1080/00207454.2022.2074847