- Help Line No. 011 61406300 / 011 27907000
click to get more results...
click to get more results...
Landau-Kleffner syndrome (also called infantile acquired aphasia, acquired epileptic aphasia, or aphasia with convulsive disorder) is a language disorder. It frequently occurs in normally-developing children, usually between three and seven years of age, and is characterized by the gradual or sudden loss of the ability use or comprehend spoken language.
It is a rare disorder, with approximately 160 cases diagnosed between 1957, when the syndrome was first identified, and 1990.
The following are the most common indicators of Landau-Kleffner syndrome. However, each individual may experience symptoms differently.
Approximately 80 percent of children with Landau-Kleffner syndrome have a history of one or more epileptic seizures that usually occur at night.
All children with Landau-Kleffner syndrome have abnormal electrical brain wave activity on both sides of the brain.
Hearing and intelligence usually are confirmed to be normal in children with Landau-Kleffner syndrome. However, the disorder may be accompanied by behavior or psychological problems such as:
The symptoms of Landau-Kleffner syndrome may resemble other conditions or medical problems, such as deafness or learning disabilities. Always consult your physician for a diagnosis.
Landau-Kleffner syndrome is commonly diagnosed using an electroencephalogram (EEG), a scan that shows the brain’s electrical waves, as well as other diagnostic tests.
Specific treatment for Landau-Kleffner syndrome will be determined by your physician based on:
Treatment may include medication for seizures, convulsions, and language ability. Sign-language instruction may also be suggested.