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<front>
<journal-meta>
<journal-id journal-id-type="issn">1043-3155</journal-id>
<journal-id journal-id-type="nlm-ta">Pediatr Neurol Briefs</journal-id>
<journal-id journal-id-type="pmc">pedneurbriefs</journal-id>
<journal-id journal-id-type="iso-abbrev">Pediatr Neurol Briefs</journal-id>
<journal-title-group>
<journal-title>Pediatric Neurology Briefs</journal-title>
<abbrev-journal-title>Pediatr Neurol Briefs</abbrev-journal-title>
</journal-title-group>
<issn pub-type="epub">2166-6482</issn>
<issn pub-type="ppub">1043-3155</issn>
<issn-l>2166-3155</issn-l>
<publisher>
<publisher-name>Pediatric Neurology Briefs Publishers</publisher-name>
<publisher-loc>Chicago, IL, USA</publisher-loc>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="publisher-id">PNB-13-29</article-id>
<article-id pub-id-type="doi">10.15844/pedneurbriefs-13-4-6</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Seizure Disorders</subject>
</subj-group>
<subj-group subj-group-type="Discipline-v2">
<subject>Neurology</subject>
<subject>Pediatrics</subject>
<subject>Nervous System Diseases</subject>
<subject>Child Development</subject>
<subject>Brain Diseases</subject>
<subject>Neurosurgery</subject>
<subject>Child</subject>
<subject>Infant</subject>
</subj-group>
</article-categories>
<title-group>
<article-title>Subpial Resection for Landau-Kleffner Syndrome</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author" corresp="yes">
<contrib-id contrib-id-type="orcid">http://orcid.org/0000-0002-0173-7931</contrib-id>
<name>
<surname>Millichap</surname>
<given-names>J. Gordon</given-names>
</name>
<degrees>MD</degrees>
<xref ref-type="aff" rid="AF0001">1</xref>
<xref ref-type="aff" rid="AF0002">2</xref>
<xref ref-type="corresp" rid="cor1">&#x002A;</xref>
</contrib>
</contrib-group>
<aff id="AF0001">
<label>1</label>Division of Neurology, Children&#x0027;s Memorial Hospital, Chicago, IL</aff>
<aff id="AF0002">
<label>2</label>Departments of Pediatrics and Neurology, Northwestern University Feinberg School of Medicine, Chicago, IL</aff>
<author-notes>
<corresp id="cor1"><label>&#x002A;</label>Correspondence: Dr. J. Gordon Millichap, E-mail: <email xlink:href="jgmillichap@northwestern.edu">jgmillichap@northwestern.edu</email>
</corresp>
</author-notes>
<pub-date date-type="pub" publication-format="print">
<month>04</month>
<year>1999</year>
</pub-date>
<pub-date date-type="pub" publication-format="electronic">
<day>01</day>
<month>05</month>
<year>2016</year>
</pub-date>
<volume>13</volume>
<issue>4</issue>
<fpage>29</fpage>
<lpage>30</lpage>
<permissions>
<copyright-statement>Copyright: &#x00A9; 1999 The Author(s)</copyright-statement>
<copyright-year>1999</copyright-year>
<license license-type="open-access" xlink:href="http://creativecommons.org/licenses/by/4.0/">
<license-p>This work is licensed under the <uri xlink:href="http://creativecommons.org/licenses/by/4.0/">Creative Commons Attribution 4.0 International License</uri>, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.</license-p>
</license>
</permissions>
<related-article id="R1" related-article-type="commentary-article" ext-link-type="doi" xlink:href="10.1093/brain/122.3.561" vol="122" page="561">
<article-title>Language outcome following multiple subpial transection for Landau-Kleffner syndrome</article-title>
</related-article>
<abstract abstract-type="web-summary" specific-use="electronic-only">
<p>Speech and language outcome of 14 children treated for Landau-Kleffner syndrome by multiple subpial transection was evaluated at Rush-Prebyterian-St Luke&#x2019;s Medical Center, Chicago.</p>
</abstract>
<kwd-group>
<kwd>Subpial Transection</kwd>
<kwd>Cognitive Development</kwd>
<kwd>Developed Meningitis</kwd>
</kwd-group>
</article-meta>
</front>
<body>
<p>Speech and language outcome of 14 children treated for Landau-Kleffner syndrome by multiple subpial transection was evaluated at Rush-Prebyterian-St Luke&#x2019;s Medical Center, Chicago. Language deficits presented at a mean age of 4 years, with a range of 3.0-6.5 yrs, and previous history of language and cognitive development was normal. The average age at time of surgery was 7.4 years, and the range was 5 to 13 years. Two patients had surgical complications; one developed meningitis and another suffered a stroke. Eleven (79%) had significant postoperative improvement in receptive and expressive vocabulary. The extent of improvement was inversely correlated with age of onset and age of surgery, and directly correlated with the time elapsed between surgery and the time of the most recent postoperative language evaluation. A control group was not available. [<xref ref-type="bibr" rid="CIT0001">1</xref>]</p>
<p>COMMENT. Landau-Kleffner syndrome is an acquired epileptic aphasia that develops in previously normal young children who lose previously acquired speech and language abilities. All patients selected for the study met these diagnostic criteria. The best predictor of language outcome following subpial resection was the amount of time elapsed between surgery and the time of language evaluation. In the absence of a control group, could these results be a function of the natural history of the disease? The following reports suggest that, although the Rush-Presbyterian experience is encouraging, controls may be needed to accurately evaluate the benefits of subpial resection.</p>
<p>Deonna T and associates of Lausanne, Switzerland, have reported an adult follow-up study of 7 patients with acquired epileptic aphasia beginning in childhood [<xref ref-type="bibr" rid="CIT0002">2</xref>]. Four showed no improvement, two were partially improved, and one man had made a complete recovery of speech and language. These authors subsequently reported a patient followed from age 3 to 18 years whose language and behavior correlated with abnormalities on the EEC Improvement coincided with the disappearance of continuous spike wave during sleep and the onset of a unilateral focus [<xref ref-type="bibr" rid="CIT0003">3</xref>]. Paquier PF et al, Rotterdam, The Netherlands, in a follow-up of 6 patients for periods ranging from 3 to 19 years found the outcome of aphasia variable, with slow improvement in 4, rapid recovery in 1, and fluctuating course in 1 [<xref ref-type="bibr" rid="CIT0004">4</xref>]. (see <underline>Progress in Pediatric Neurology I</underline>. PNB Publishers, 1991;pp217-218; and Vol II, 1994;pp57-58, for several references and commentary regarding outcome of L-K syndrome).</p>
<p><bold>Landau-Kleffner syndrome (LKS) and electrical status epilepticus during sleep (ESES)</bold>. Eleven patients with LKS and bitemporal ESES were followed for a mean of 9 yrs and 8 mos at the Neurological Institute, University of Bologna, Italy. Complete recovery of language and cognitive abilities occurred in 18%, and 64% were mentally retarded. Poor outcome showed some relation to onset of aphasia before 4 years, duration for longer than 1 year, and long-lasting ESES, probably preexisting speech delay. The common origin of LKS and ESES is confirmed by recent functional brain imaging studies. The elimination of ESES appears to be important in prognosis of LKS. [<xref ref-type="bibr" rid="CIT0005">5</xref>]</p>
</body>
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