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Landau-Kleffner Syndrome – Case Report

Stanislav Rogulja ; Klinički bolnički centar Osijek, Zavod za dječju i adolescentnu psihijatriju, Osijek, Hrvatska
Marina Bježančević ; Klinički bolnički centar Osijek, Zavod za dječju i adolescentnu psihijatriju, Osijek, Hrvatska
Petra Horvat ; Klinički bolnički centar Osijek, Zavod za dječju i adolescentnu psihijatriju, Osijek, Hrvatska
Katarina Dodig-Ćurković ; Klinički bolnički centar Osijek, Zavod za dječju i adolescentnu psihijatriju, Osijek, Hrvatska, Sveučilište Josipa Jurja Strossmayera u Osijeku, Medicinski fakultet, Osijek, Hrvatska, Fakultet za dentalnu medicinu i zdravstvo, Osijek, Hrvatska


Puni tekst: hrvatski pdf 134 Kb

str. 113-125

preuzimanja: 401

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Puni tekst: engleski pdf 134 Kb

str. 113-125

preuzimanja: 2.576

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Sažetak

Landau-Kleffner syndrome is an epileptic childhood syndrome and is synonymous with acquired epileptic aphasia. Since 1957, when Landau and Kleffner identified six children with the disorder, more than 350 cases worldwide have been reported. The specificity of Landau Kleffner syndrome is an acute loss of speech and language in a child who
developed normal language and global regression of behaviour. The rarity of this syndrome makes it extremely demanding to diagnose. It requires a multidisciplinary treatment by specialists in the field of pediatrics, neuropediatrics, child psychiatry, psychology, logopedia, otorhinolaryngology, and brain imaging. The final diagnosis is based on an epileptogenically altered EEG finding during sleep with an orderly brain MRI finding, along with clinical manifestations of the syndrome. This paper describes a multidisciplinary treatment, early initiation of treatment, and further course of illness.

Ključne riječi

Landau-Kleffner syndrome; Acquired epileptic aphasia

Hrčak ID:

218772

URI

https://hrcak.srce.hr/218772

Datum izdavanja:

5.4.2019.

Podaci na drugim jezicima: hrvatski

Posjeta: 4.886 *