What is Landau-Kleffner Syndrome?
Landau-Kleffner Syndrome (LKS), also known as acquired epileptic aphasia or infantile acquired aphasia, is a rare neurological disorder that primarily affects children.
It is characterized by the gradual or sudden loss of language skills, typically between the ages of 3 and 7 years old.
Children with Landau-Kleffner Syndrome may experience a regression in their ability to understand and use spoken language, as well as difficulties in interpreting and producing words.
Side Effects of Landau-Kleffner Syndrome
Apart from the core symptom of language regression, children with LKS may also exhibit other neurological issues such as seizures, behavioral problems, and difficulties with social interaction.
These additional symptoms can significantly impact a child's overall development and quality of life.
How is Landau-Kleffner Syndrome Diagnosed?
Diagnosing Landau-Kleffner Syndrome can be challenging due to its rarity and the variability of symptoms. Typically, a comprehensive evaluation by a neurologist or pediatric neurologist is necessary. Diagnostic tests may include:
Potential Treatment of Landau-Kleffner Syndrome
Treatment for Landau-Kleffner Syndrome typically involves a multidisciplinary approach tailored to the individual needs of the child. Some common treatment strategies may include:
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