A rare case of antileucine-rich glioma-inactivated 1 encephalitis in a 14-year-old girl.
Turk J Pediatr
; 64(3): 566-570, 2022.
Article
em En
| MEDLINE
| ID: mdl-35899570
ABSTRACT
BACKGROUND:
Autoimmune limbic encephalitis in children occurs most frequently in those with antibodies against the N-methyl-D-aspartate glutamatergic receptor. We report the case of a 14-year-old girl who was diagnosed with antileucine-rich glioma-inactivated protein 1 limbic encephalitis. CASE A fourteen years old, previously healthy girl applied to the emergency department with suspicion of dystonic seizure, ataxia, gait disturbance and speech disorders. Serum sample of the patient was positive for leucine-rich glioma inactivated protein 1 IgG.CONCLUSIONS:
Although it is a rare disease in childhood, in the presence of new onset psychotic symptoms or altered mental state, concomittant hyponatremia and unique type of seizures, anti leucine-rich glioma inactivated protein 1encephalitis should be considered in differential diagnosis.Palavras-chave
Texto completo:
1
Coleções:
01-internacional
Base de dados:
MEDLINE
Assunto principal:
Encefalite Límbica
/
Encefalite
/
Glioma
Tipo de estudo:
Diagnostic_studies
/
Etiology_studies
Limite:
Adolescent
/
Child
/
Female
/
Humans
Idioma:
En
Revista:
Turk J Pediatr
Ano de publicação:
2022
Tipo de documento:
Article
País de afiliação:
Turquia