Vol. 26 - Num. 104
Clinical Reviews
Alberto Bercedo Sanza, Sandra Alonso Badab, Roberto Ocón Quintialc, M.ª Teresa Castro García-Montesinosd, Andrea Sariego Jamardoe, Aurora Pérez Guerrerof
aPediatra. CS Los Castros. Instituto de Investigación Sanitaria Valdecilla (IDIVAL). Santander. Cantabria. España
bPsiquiatra infantil. Unidad de Salud Mental Infanto-Juvenil. Torrelavega. Cantabria. España.
cNeurofisiólogo. Hospital Universitario Marqués de Valdecilla. Santander. Cantabria. España.
dMIR-Pediatría. Hospital Universitario Marqués de Valdecilla. Santander. Cantabria. España.
eNeuropediatra. Hospital Universitario Marqués de Valdecilla. Santander. Cantabria. España
fPediatra. CS Buelna. Los Corrales de Buelna. Cantabria. España.
Correspondence: A Bercedo. E-mail: drbercedo@gmail.com
Reference of this article: Bercedo Sanz A, Alonso Bada S, Ocón Quintial R, Castro García-Montesinos MT, Sariego Jamardo A, Pérez Guerrero A. It looks like encephalitis, but it is Kleine-Levin syndrome . Rev Pediatr Aten Primaria. 2024;26:389-92. https://doi.org/10.60147/ab42fc5c
Published in Internet: 03-12-2024 - Visits: 1158
Abstract
Kleine-Levin syndrome is a rare disease characterized by recurrent episodes of hypersomnia and cognitive and behavioural changes. We present the case of a female patient aged 13 years who, following infection by influenza A virus, presented with disorientation, incoherent speech, bradypsychia, behavioural changes, somnolence and apathy. No history of trauma or toxic substance exposure. Kleine-Levin or “sleeping beauty” syndrome has an unknown aetiology and a good prognosis with progressive resolution with age. There is no curative treatment, but corticosteroids have been used during episodes and preventive treatments like lithium and modafinil.
Keywords
● Encephalitis ● Hypersomnia ● Kleine-Levin Syndrome ● Rare diseases ● Sleep disordersComments
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