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| __NOTOC__
| | #REDIRECT [[Landau-Kleffner_syndrome]] |
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| {{Infobox disease |
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| Name = Landau–Kleffner syndrome |
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| Image = Eeg raw.svg |
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| Caption = Landau–Kleffner syndrome is characterized by [[aphasia]] and an abnormal [[Electroencephalography|EEG]]|
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| ICD10 = {{ICD10|F|80|3|f|80}} |
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| ICD9 = {{ICD9|345.8}} |
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| ICDO = |
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| OMIM = 245570 |
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| DiseasesDB = 31407 |
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| MedlinePlus = |
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| MeshID = D018887 |
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| }}
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| {{CMG}}
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| '''''synonyms and keywords:''''' infantile acquired aphasia, acquired epileptic aphasia,
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| == Etymology ==
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| It is named after William Landau and Frank Kleffner, who characterized it in 1957 with a diagnosis of six children.
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| == Presentation ==
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| It is characterized by the sudden or gradual development of [[aphasia]] (the inability to understand or express language) and an abnormal [[Electroencephalography|electroencephalogram]] (EEG).<ref name="pmid15309183">{{cite journal |author=Pearl PL, Carrazana EJ, Holmes GL |title=The Landau–Kleffner Syndrome |journal=Epilepsy Curr |volume=1 |issue=2 |pages=39–45 |year=2001 |month=November |pmid=15309183 |pmc=320814 |doi=10.1046/j.1535-7597.2001.00012.x |url=}}</ref> LKS affects the parts of the brain that control comprehension and speech ([[Broca's area]] and [[Wernicke's area]]). The disorder usually occurs in children between the ages of 3 and 7 years. There appears to be a slight male dominance in the diagnosis of the syndrome (ration of 1.7:1, men to women).<ref name="emedicine">{{cite web |url=http://emedicine.medscape.com/article/1176568-overview |title=Acquired Epileptic Aphasia |format=medicinenet |work=Medscape part of WebMD Health Professional Network |accessdate=}}</ref>
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| Typically, children with LKS develop normally, but then lose their language skills. While many affected individuals have clinical seizures, some only have electrographic seizures, including electrographic status epilepticus of sleep (ESES). The first indication of the language problem is usually [[auditory verbal agnosia]]. This is demonstrated in patients in multiple ways including the inability to recognize familiar noises and the impairment of the ability to lateralize or localize sound. In addition, receptive language is often critically impaired, however in some patients, impairment in expressive language is the most profound. In a study of 77 cases of Landau–Kleffner syndrome, 6 were found to have this type of aphasia. Because this syndrome appears during such a critical period of language acquisition in a child's life, speech production may be affected just as severely as language comprehension.<ref name="emedicine"/> The onset of LKS is typically between 18 months and 13 years, the most predominant time of emergence being between 3 and 7 years.
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| Generally, earlier manifestation of the disease correlates with poorer language recovery, and with the appearance of night seizures that last for longer than 36 months.<ref name= "emedicine"/> LKS has a wide range of symptom differences and lacks a uniformity in diagnostic criteria between cases, and many studies don't include follow-ups on the patients, so no other relationships between symptoms and recovery have been made known.<ref name="medicinenet"/>
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| Language deterioration in patients typically occurs over a period of weeks or months. However, acute onset of the condition has also been reported as well as episodic aphasia.
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| Seizures, especially during the night, are a heavily weighted indicator of LKS. The prevalence of clinical seizures in acquired epileptic aphasia (LKS) is 70-85%. In one third of patients, only a single episode of a seizure was recorded. The seizures typically appear between the ages of 4 and 10 and disappear before adulthood (around the age of 15).<ref name="emedicine"/>
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| Often, behavioral and neuropsychologic disturbances accompany the progression of LKS. Behavioral issues are seen in as many as 78% of all cases. Hyperactivity and a decreased attention span are observed in as many as 80% of patients as well as rage, aggression, and anxiety. These behavior patterns are considered secondary to the language impairment in LKS. Impaired short-term memory is a feature recorded in long-standing cases of acquired epileptic aphasia.<ref name= "emedicine"/>
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| The table below demonstrates the extensive and differential diagnosis of acquired epileptic aphasia along with Cognitive and Behavioral Regression:<ref name= "emedicine"/>
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| {| class="wikitable"
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| ! Diagnosis !! Deterioration !! EEG Patterns
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| | Autistic epileptiform regression || Expressive language, RL, S, verbal and nonverbal communication || Centrotemporal spikes
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| | Autistic regression || Expressive language, RL, S, verbal and nonverbal communication || Normal
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| | Acquired epileptic aphasia || RL, possibly behavioral || Left or right temporal or parietal spikes, possibly ESES
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| | Acquired expressive epileptic aphasia || Expressive language, oromotor apraxia || Centrotemporal spikes
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| | ESES) || Expressive language, RL, possibly behavioral || ESES
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| | Developmental dysphasia (developmental expressive language disease) || No; lack of expressive language acquisition || Temporal or parietal spikes
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| | Disintegrative epileptiform disorder || Expressive language, RL, S, verbal and nonverbal communication, possibly behavioral || ESES
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| |}
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| Note: EEG = electroencephalographic; ESES = electrical status epilepticus of sleep; RL = receptive language; S = sociability
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| * Continuous spike and wave of slow-wave sleep (>85% of slow-wave sleep).
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| == Prognosis ==
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| The prognosis for children with LKS varies. Some affected children may have a permanent severe language disorder, while others may regain much of their language abilities (although it may take months or years). In some cases, remission and relapse may occur. The prognosis is improved when the onset of the disorder is after age 6 and when speech therapy is started early. Seizures generally disappear by adulthood. Short-term remissions are not uncommon in LKS but they create difficulties in evaluating a patient's response to various therapeutic modalities.
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| The following table demonstrate the Long-Term Follow-up of Acquired Epileptic Aphasia across many different instrumental studies:.<ref name="emedicine"/>
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| {| class="wikitable"
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| ! Study !! Number of Patients !! Mean Follow-up, y !! Number of Patients with Normal or Mild Language Problems
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| | Soprano ''et al.'' (1994) || 12 || 8 || 3
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| | Mantovani and Landau (1980) || 9 || 22 || 6
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| | Paquier (1992) || 6 || 8.1 || 3
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| | Rossi (1999) || 11 || 9.7 || 2
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| | Robinson et all (2001) || 18 || 5.6 || 3
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| | Duran ''et al.'' (2009) || 7 || 9.5 || 1
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| | Total || 63 || || 18 (28.6%)
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| |}
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| Lower rates of good outcomes have been reported, ranging between 14% to 50%. Duran ''et al.'' used 7 patients in his study (all males, aged 8–27 years of age) with LKS. On long-term followup, most of his patients did not demonstrate total epilepsy remission and language problems continued. Out of the seven patients, one reported a normal quality of life while the other six reported aphasia to be a substantial struggle. The Duran ''et al.'' study is one of few that features long-term follow up reports of LKS and utilizes EEG testing, MRIs, the Vineland Adaptive Behavior Scales, the Connor's Rating Scales-revised, and a Short-Form Health Survey to analyze its patients.<ref name="Duran, 2009">{{cite journal |author=Duran MH, Guimarães CA, Medeiros LL, Guerreiro MM |title=Landau-Kleffner syndrome: long-term follow-up |journal=Brain Dev. |volume=31 |issue=1 |pages=58–63 |year=2009 |month=January |pmid=18930363 |doi=10.1016/j.braindev.2008.09.007 |url=}}</ref>
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| Globally, more than 200 cases of LKS have been reported. Between 1957 and 1980, 81 cases were reported with 100 cases generally being reported every 10 years.<ref name="emedicine"/>
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| == Differential diagnosis ==
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| The syndrome can be difficult to diagnose and may be misdiagnosed as [[autism]], pervasive developmental disorder, hearing impairment, learning disability, auditory/verbal processing disorder, [[Attention-deficit hyperactivity disorder|attention deficit disorder]], mental retardation, childhood [[schizophrenia]], or emotional/behavioral problems. An EEG (electroencephalogram) test is imperative to a diagnosis. Many cases of patients exhibiting LKS will show abnormal electrical brain activity in both the right and left hemispheres of the brain; this is exhibited frequently during sleep.<ref name="medicinenet"/> Even though an abnormal EEG reading is common in LKS patients, a relationship has not been identified between EEG abnormalities and the presence and intensity of language problems. In many cases however, abnormalities in the EEG test has preceded language deterioration and improvement in the readings has preceded language improvement (this occurs in about half of all affected children). Many factors inhibit the reliability of the EEF date: neurologic deficits do no closely follow the maximal EEG changes in time.<ref name="emedicine"/>
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| The most effective way of confirming LKS is by obtaining overnight sleep EEGs, including EEGs in all stages of sleep. Many conditions like demyelination and brain tumors can be ruled out by using magnetic resonance imaging (MRI). In LKS, fluorodeoxyglucose (FDG) and positron emission tomography (PET) scanning can show decreased metabolism in one or both temporal lobes - hypermetabolism has been seen in patients with acquire epileptic aphasia.<ref name="emedicine"/>
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| Most cases of LKS do not have a known cause. Occasionally, the condition may be induced secondary to other diagnoses such as low-grade brain tumors, closed-head injury, [[neurocysticercosis]], and [[demyelinating disease]]. Central Nervous System vasculitis may be associated with this condition as well.<ref name="emedicine"/>
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| == Treatment ==
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| Treatment for LKS usually consists of medications, such as [[anticonvulsant]]s<ref name="pmid17557221">{{cite journal |author=Guevara-Campos J, González-de Guevara L |title=Landau–Kleffner syndrome: an analysis of 10 cases in Venezuela |language=Spanish; Castilian |journal=Rev Neurol |volume=44 |issue=11 |pages=652–6 |year=2007 |pmid=17557221 |doi= |url=http://www.revneurol.com/LinkOut/formMedLine.asp?Refer=2006465&Revista=RevNeurol}}</ref> and [[corticosteroid]]s<ref name="pmid15866429">{{cite journal |author=Sinclair DB, Snyder TJ |title=Corticosteroids for the treatment of Landau–Kleffner syndrome and continuous spike-wave discharge during sleep |journal=Pediatr. Neurol. |volume=32 |issue=5 |pages=300–6 |year=2005 |month=May |pmid=15866429 |doi=10.1016/j.pediatrneurol.2004.12.006 |url=http://linkinghub.elsevier.com/retrieve/pii/S0887-8994(05)00030-5}}</ref> (such as [[prednisone]]),<ref name="pmid12068352">{{cite journal |author=Santos LH, Antoniuk SA, Rodrigues M, Bruno S, Bruck I |title=Landau–Kleffner syndrome: study of four cases |journal=Arq Neuropsiquiatr |volume=60 |issue=2–A |pages=239–41 |year=2002 |month=June |pmid=12068352 |doi= |url=http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0004-282X2002000200010&lng=en&nrm=iso&tlng=en}}</ref> and [[speech therapy]], which should be started early. Some patients improve with the use of corticosteroids or adrenocorticotropin hormone (ACTH) which lead researches to believe that inflammation and vasospasm may play a role in some cases of acquired epileptic aphasia.<ref name= "emedicine" />
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| A controversial treatment option involves a surgical technique called [[multiple subpial transection]]<ref name="pmid10094262">{{cite journal |author=Grote CL, Van Slyke P, Hoeppner JA |title=Language outcome following multiple subpial transection for Landau–Kleffner syndrome |journal=Brain |volume=122 |issue= 3|pages=561–6 |year=1999 |month=March |pmid=10094262 |doi= |url=http://brain.oxfordjournals.org/cgi/pmidlookup?view=long&pmid=10094262}}</ref> in which multiple incisions are made through the [[Cerebral cortex|cortex]] of the affected part of the [[brain]] beneath the [[pia mater]], severing the [[axon]]al tracts in the subjacent [[white matter]]. The cortex is sliced in parallel lines to the midtemporal gyrus and perisylvian area to attenuate the spread of the epileptiform activity without causing cortical dysifunction. There is a study by Morrell ''et al.'' in which results were reported for 14 patients with acquired epileptic aphasia who underwent multiple subpial transections. Seven of the fourteen patients recovered age-appropriate speech and no longer required speech therapy. Another 4 of the 14 displayed improvement of speech and understanding instructions given verbally, but they still required speech therapy. Eleven patients had language dysfunction for two or more years.<ref name="Morrell, 1995" >{{cite journal |author=Morrell F, Whisler WW, Smith MC, ''et al.'' |title=Landau-Kleffner syndrome. Treatment with subpial intracortical transection |journal=Brain |volume=118 ( Pt 6) |issue= |pages=1529–46 |year=1995 |month=December |pmid=8595482 |doi=10.1093/brain/118.6.1529 |url=}}</ref> Another study by Sawhney ''et al.'' reported improvement in all three of their patients with acquired epileptic aphasia who underwent the same procedure.<ref name="Sawhney, 1995">{{cite journal |author=Sawhney IM, Robertson IJ, Polkey CE, Binnie CD, Elwes RD |title=Multiple subpial transection: a review of 21 cases |journal=J. Neurol. Neurosurg. Psychiatr. |volume=58 |issue=3 |pages=344–9 |year=1995 |month=March |pmid=7897419 |pmc=1073374 |doi= |url=http://jnnp.bmj.com/content/58/3/344.long}}</ref>
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| Various hospitals contain programs designed to treat conditions such as LKS like the Children's Hospital Boston and its Augmentative Communication Program. It is known internationally for its work with children or adults who are non-speaking or severely impaired. Typically, a care team of children with LKS consists of a neurologist, a neuropsychologist, and a speech pathologist or audiologist. Some children with behavioral problems may also need to see a child psychologist and a psychopharmacologist. Speech therapy begins immediately at the time of diagnosis along with medical treatment that may include steroids and anti-epileptic or anti-convulsant medications.
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| Patient education has also proved to be helpful in treating LKS. Teaching them sign language is a helpful means of communication and if the child was able to read and write before the onset of LKS, that is extremely helpful too.
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| == References ==
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| {{reflist|2}}
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| {{WH}}
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| {{WS}}
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| [[Category:Grammar]]
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| [[Category:Disease]]
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