How do you diagnose Landau-Kleffner syndrome?
Landau-Kleffner syndrome is commonly diagnosed using an electroencephalogram (EEG). This is a scan that shows the brain’s electrical waves. Other diagnostic tests may be used.
Is Landau-Kleffner syndrome autism?
Landau-Kleffner Syndrome It is twice as common in males than females and is often diagnosed in conjunction with autism. Initially, these individuals have a healthy, problem-free development with normal speech and vocabulary.
Is Landau-Kleffner syndrome a disability?
Some children with Landau-Kleffner syndrome may develop behavioral problems including hyperactivity, attention deficits, temper outbursts, impulsivity, and/or withdrawn behaviors. Some children with Landau Kleffner syndrome may also have intellectual disability .
Can Landau-Kleffner syndrome be cured?
What is the outlook for people with Landau-Kleffner syndrome? The outlook for recovering language is poor when LKS starts early in life or lasts for a long time without successful treatment. Seizures and EEG abnormalities go away in most cases.
Who discovered Landau-Kleffner?
It is named after William Landau and Frank Kleffner, who characterized it in 1957 with a diagnosis of six children.
Can genetic seizures be cured?
There’s no cure for epilepsy, but the disorder can be managed with medications and other strategies.
What causes ohtahara syndrome?
Ohtahara syndrome is classically caused by very abnormal brain structure that may be due to damage or abnormal development. It also can be due to metabolic disorders or genetic epilepsy syndromes, although the cause or causes for many cases can’t be determined.
What is Csws epilepsy?
Epilepsy with continuous spikes and waves during slow sleep (CSWS) is a rare neurological disease. CSWS is not an independent epilepsy syndrome but often accompanied by comprehensive damage of brain function and associated with various forms of epilepsy and neurodevelopmental problems.
What are the symptoms of temporal lobe damage?
Damage to the temporal lobes can result in:
- Difficulty in understanding spoken words (Receptive Aphasia)
- Disturbance with selective attention to what we see and hear.
- Difficulty with identification and categorisation of objects.
- Difficulty learning and retaining new information.
- Impaired factual and long-term memory.
What do you need to know about Landau Kleffner syndrome?
Summary Summary. Landau-Kleffner syndrome (LKS) is a rare neurological syndrome characterized by the sudden or gradual development of aphasia (the inability to understand or express language) and recurrent seizures (epilepsy).
When did Landau and Kleffner report their findings?
The correlation between paroxysmal EEG discharges and language deterioration was first suggested by Landau and Kleffner (1957), who reported five children with acquired aphasia associated with a convulsive disorder 1.
When do children with LKS lose their language skills?
LKS affects the parts of the brain that control comprehension and speech, typically affecting understanding rather than expression. The disorder usually occurs in children between the ages of 5 and 7 years. Typically, children with LKS develop normally but then lose their language skills for no apparent reason.
How is LKS related to autism spectrum disorder?
The language disorder of LKS has commonalities with autism spectrum disorder. Communication deficits in autism include abnormal development of spoken language and impaired ability to initiate or sustain conversation. The autistic child’s language is often stereotyped, repetitive, and idiosyncratic, with echolalia and neologisms 11.