Landau-Kleffner Syndrome

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PatientPlus articles are written by UK doctors and are based on research evidence, UK and European Guidelines. They are designed for health professionals to use, so you may find the language more technical than the condition leaflets.

See also: Aphasia (Dysphasia) written for patients
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Synonyms: acquired epileptic aphasia

Landau-Kleffner syndrome is an acquired aphasia secondary to an epileptic disturbance affecting a cortical area involved in verbal processing.[1] Affected children who have developed age-appropriate speech then experience language regression with verbal auditory agnosia, abnormal epileptiform activity, behavioural disturbances, and sometimes overt seizures.[2] Landau and Kleffner initially described acquired epileptic aphasia in 1957.[3] Landau-Kleffner syndrome has three features:[4]

  • An acquired receptive aphasia.
  • Temporoparietal spike-wave discharges in the awake state.
  • Frequent generalised spike-wave discharges in sleep (electrical status epilepticus in sleep (ESES)).
  • The syndrome has been thought to be very rare but, with improved diagnostic techniques, the known prevalence may increase significantly.
  • Currently, over 200 cases have been described in world literature.
  • There is a slight increase in incidence in boys.
  • Most cases do not have a well-defined cause. A few cases appear to have been secondary to low-grade brain tumours, closed head injury, neurocysticercosis and demyelinating disease.

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  • Onset of aphasia is usually between the ages of 3 and 8 years.
  • The syndrome is typically characterised by an abrupt or gradual loss of language ability and inattentiveness to sound (auditory agnosia).
  • Receptive language is often severely impaired.
  • Reading and writing may be preserved.
  • The child may be completely mute or have severe expressive speech problems.
  • Seizures occur in most cases and usually present between the ages of 4 and 10 years.
  • Seizures may be partial, generalised tonic-clonic, absence or myoclonic.
  • Many affected children have behavioural disturbances, including hyperactivity and decreased attention span, aggression and attacks of rage.
  • MRI is essential to rule out cerebrovascular thromboembolism, brain tumours, demyelination, neurodegenerative disease and central nervous system infections.
  • Fluorodeoxyglucose positron emission tomography (FDG-PET) imaging reveals decreased metabolism in one or both temporal lobes. Single-photon emission computed tomography (SPECT) of the brain demonstrates decreased perfusion of the left temporal lobe.
  • EEG: abnormalities are present in this syndrome but no consensus exists about what constitutes typical abnormalities.
  • Brainstem auditory evoked potentials and hearing tests.
  • Patients have special educational needs and require speech therapy. Speech therapy, including sign language, and a number of classroom and behavioural interventions, is beneficial.[2]
  • Psychotherapy may be indicated.
  • A ketogenic diet has been recommended but experience is very limited.


  • Anticonvulsant medications have variable success.
  • As initial therapy, valproic acid or diazepam is often used. Subsequently, other anti-epileptic drugs, corticosteroids, or intravenous immunoglobulin (IVIG) therapy are often used.
  • Various corticosteroid regimens including oral prednisone, high doses of intravenous pulse corticosteroids, and adrenocorticotrophic hormone (ACTH) have been reported to be effective.[2]


Multiple subpial transection (MST) has been used:[5]

  • The cortex is sliced in parallel lines in the midtemporal gyrus and perisylvian area in order to prevent the spread of the epileptiform activity without causing cortical dysfunction.
  • This treatment is reserved for patients who have not responded to multiple medical therapies, but has been followed in selected cases by a marked improvement in language skills and behaviour.
  • There is currently no accepted consensus about suitable candidates for this procedure or evidence for its effectiveness.[2]

The long-term follow-up shows that epilepsy and EEG abnormalities do not always disappear. Language disturbances tend to persist in most patients. Patients tend to have an overall poor quality of life, mostly due to language difficulties.[6]

  • The overall long-term prognosis for language development is poor.[7] Between 25% and 50% maintain language function at a level good enough to hold a job and have a normal social life.[3]
  • Patients with an onset of language regression before the age of 5 years may have a worse prognosis and symptoms persisting for more than one year are predictive of poor language recovery.[3]
  • Fluctuations in clinical severity and EEG changes are not unusual and short-term remissions may occur.[3]

Further reading & references

  1. Hirsch E, Valenti MP, Rudolf G, et al; Landau-Kleffner syndrome is not an eponymic badge of ignorance. Epilepsy Res. 2006 Aug;70 Suppl 1:S239-47. Epub 2006 Jun 27.
  2. Mikati MA, Shamseddine AN; Management of Landau-Kleffner syndrome. Paediatr Drugs. 2005;7(6):377-89.
  3. Neiman ES et al; Landau-Kleffner Syndrome, eMedicine, Jul 2010
  4. Landau Kleffner Syndrome, Epilepsy in action
  5. Sawhney IM, Robertson IJ, Polkey CE, et al; Multiple subpial transection: a review of 21 cases. J Neurol Neurosurg Psychiatry. 1995 Mar;58(3):344-9.
  6. Duran MH, Guimaraes CA, Medeiros LL, et al; Landau-Kleffner syndrome: long-term follow-up. Brain Dev. 2009 Jan;31(1):58-63. Epub 2008 Oct 17.
  7. Soprano AM, Garcia EF, Caraballo R, et al; Acquired epileptic aphasia: neuropsychologic follow-up of 12 patients. Pediatr Neurol. 1994 Oct;11(3):230-5.

Disclaimer: This article is for information only and should not be used for the diagnosis or treatment of medical conditions. EMIS has used all reasonable care in compiling the information but make no warranty as to its accuracy. Consult a doctor or other health care professional for diagnosis and treatment of medical conditions. For details see our conditions.

Original Author:
Dr Colin Tidy
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Document ID:
1449 (v22)
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