Life‐threatening dystonia–dyskinesias in a child: Successful treatment with bilateral pallidal stimulation
Identifieur interne : 003947 ( Istex/Corpus ); précédent : 003946; suivant : 003948Life‐threatening dystonia–dyskinesias in a child: Successful treatment with bilateral pallidal stimulation
Auteurs : Lucia Angelini ; Nardo Nardocci ; Margherita Estienne ; Chiara Conti ; Ivano Dones ; Giovanni BroggiSource :
- Movement Disorders [ 0885-3185 ] ; 2000-09.
English descriptors
Abstract
We report a 13‐year‐old boy who developed severe, refractory dystonia–dyskinesias as an abrupt worsening of a previously nonprogressive movement disorder. The movements became continuous, requiring artificial respiration and continuous sedation in the intensive‐care unit. Various drugs and drug combinations failed to achieve control. The child was then treated successfully with bilateral pallidal (GPi) stimulation as shown in the videotape. Four months later and without medication, the boy regained autonomous gait and audible speech; his neurologic condition continues to improve.
Url:
DOI: 10.1002/1531-8257(200009)15:5<1010::AID-MDS1039>3.0.CO;2-5
Links to Exploration step
ISTEX:E6182ED5DFEB2ABD4405F44F80898F66B7D3B038Le document en format XML
<record><TEI wicri:istexFullTextTei="biblStruct"><teiHeader><fileDesc><titleStmt><title xml:lang="en">Life‐threatening dystonia–dyskinesias in a child: Successful treatment with bilateral pallidal stimulation</title><author><name sortKey="Angelini, Lucia" sort="Angelini, Lucia" uniqKey="Angelini L" first="Lucia" last="Angelini">Lucia Angelini</name><affiliation><mods:affiliation>Departments of Neuropediatrics and Neurosurgery, National Neurological Institute “C. Besta,” Milan, Italy</mods:affiliation></affiliation></author><author><name sortKey="Nardocci, Nardo" sort="Nardocci, Nardo" uniqKey="Nardocci N" first="Nardo" last="Nardocci">Nardo Nardocci</name><affiliation><mods:affiliation>Departments of Neuropediatrics and Neurosurgery, National Neurological Institute “C. Besta,” Milan, Italy</mods:affiliation></affiliation></author><author><name sortKey="Estienne, Margherita" sort="Estienne, Margherita" uniqKey="Estienne M" first="Margherita" last="Estienne">Margherita Estienne</name><affiliation><mods:affiliation>Departments of Neuropediatrics and Neurosurgery, National Neurological Institute “C. Besta,” Milan, Italy</mods:affiliation></affiliation></author><author><name sortKey="Conti, Chiara" sort="Conti, Chiara" uniqKey="Conti C" first="Chiara" last="Conti">Chiara Conti</name><affiliation><mods:affiliation>Departments of Neuropediatrics and Neurosurgery, National Neurological Institute “C. Besta,” Milan, Italy</mods:affiliation></affiliation></author><author><name sortKey="Dones, Ivano" sort="Dones, Ivano" uniqKey="Dones I" first="Ivano" last="Dones">Ivano Dones</name><affiliation><mods:affiliation>Department of Neurosurgery, National Neurological Institute “C. Besta,” Milan, Italy</mods:affiliation></affiliation></author><author><name sortKey="Broggi, Giovanni" sort="Broggi, Giovanni" uniqKey="Broggi G" first="Giovanni" last="Broggi">Giovanni Broggi</name><affiliation><mods:affiliation>Department of Neurosurgery, National Neurological Institute “C. Besta,” Milan, Italy</mods:affiliation></affiliation></author></titleStmt><publicationStmt><idno type="wicri:source">ISTEX</idno><idno type="RBID">ISTEX:E6182ED5DFEB2ABD4405F44F80898F66B7D3B038</idno><date when="2000" year="2000">2000</date><idno type="doi">10.1002/1531-8257(200009)15:5<1010::AID-MDS1039>3.0.CO;2-5</idno><idno type="url">https://api.istex.fr/document/E6182ED5DFEB2ABD4405F44F80898F66B7D3B038/fulltext/pdf</idno><idno type="wicri:Area/Istex/Corpus">003947</idno></publicationStmt><sourceDesc><biblStruct><analytic><title level="a" type="main" xml:lang="en">Life‐threatening dystonia–dyskinesias in a child: Successful treatment with bilateral pallidal stimulation</title><author><name sortKey="Angelini, Lucia" sort="Angelini, Lucia" uniqKey="Angelini L" first="Lucia" last="Angelini">Lucia Angelini</name><affiliation><mods:affiliation>Departments of Neuropediatrics and Neurosurgery, National Neurological Institute “C. Besta,” Milan, Italy</mods:affiliation></affiliation></author><author><name sortKey="Nardocci, Nardo" sort="Nardocci, Nardo" uniqKey="Nardocci N" first="Nardo" last="Nardocci">Nardo Nardocci</name><affiliation><mods:affiliation>Departments of Neuropediatrics and Neurosurgery, National Neurological Institute “C. Besta,” Milan, Italy</mods:affiliation></affiliation></author><author><name sortKey="Estienne, Margherita" sort="Estienne, Margherita" uniqKey="Estienne M" first="Margherita" last="Estienne">Margherita Estienne</name><affiliation><mods:affiliation>Departments of Neuropediatrics and Neurosurgery, National Neurological Institute “C. Besta,” Milan, Italy</mods:affiliation></affiliation></author><author><name sortKey="Conti, Chiara" sort="Conti, Chiara" uniqKey="Conti C" first="Chiara" last="Conti">Chiara Conti</name><affiliation><mods:affiliation>Departments of Neuropediatrics and Neurosurgery, National Neurological Institute “C. Besta,” Milan, Italy</mods:affiliation></affiliation></author><author><name sortKey="Dones, Ivano" sort="Dones, Ivano" uniqKey="Dones I" first="Ivano" last="Dones">Ivano Dones</name><affiliation><mods:affiliation>Department of Neurosurgery, National Neurological Institute “C. Besta,” Milan, Italy</mods:affiliation></affiliation></author><author><name sortKey="Broggi, Giovanni" sort="Broggi, Giovanni" uniqKey="Broggi G" first="Giovanni" last="Broggi">Giovanni Broggi</name><affiliation><mods:affiliation>Department of Neurosurgery, National Neurological Institute “C. Besta,” Milan, Italy</mods:affiliation></affiliation></author></analytic><monogr></monogr><series><title level="j">Movement Disorders</title><title level="j" type="abbrev">Mov. Disord.</title><idno type="ISSN">0885-3185</idno><idno type="eISSN">1531-8257</idno><imprint><publisher>John Wiley & Sons, Inc.</publisher><pubPlace>New York</pubPlace><date type="published" when="2000-09">2000-09</date><biblScope unit="vol">15</biblScope><biblScope unit="issue">5</biblScope><biblScope unit="page" from="1010">1010</biblScope><biblScope unit="page" to="1012">1012</biblScope></imprint><idno type="ISSN">0885-3185</idno></series><idno type="istex">E6182ED5DFEB2ABD4405F44F80898F66B7D3B038</idno><idno type="DOI">10.1002/1531-8257(200009)15:5<1010::AID-MDS1039>3.0.CO;2-5</idno><idno type="ArticleID">MDS1039</idno></biblStruct></sourceDesc><seriesStmt><idno type="ISSN">0885-3185</idno></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Deep brain stimulation</term><term>Pallidal stimulation</term><term>Refractory dyskinesia</term><term>Refractory dystonia</term></keywords></textClass><langUsage><language ident="en">en</language></langUsage></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">We report a 13‐year‐old boy who developed severe, refractory dystonia–dyskinesias as an abrupt worsening of a previously nonprogressive movement disorder. The movements became continuous, requiring artificial respiration and continuous sedation in the intensive‐care unit. Various drugs and drug combinations failed to achieve control. The child was then treated successfully with bilateral pallidal (GPi) stimulation as shown in the videotape. Four months later and without medication, the boy regained autonomous gait and audible speech; his neurologic condition continues to improve.</div></front></TEI><istex><corpusName>wiley</corpusName><author><json:item><name>Lucia Angelini MD</name><affiliations><json:string>Departments of Neuropediatrics and Neurosurgery, National Neurological Institute “C. Besta,” Milan, Italy</json:string></affiliations></json:item><json:item><name>Nardo Nardocci MD</name><affiliations><json:string>Departments of Neuropediatrics and Neurosurgery, National Neurological Institute “C. Besta,” Milan, Italy</json:string></affiliations></json:item><json:item><name>Margherita Estienne MD</name><affiliations><json:string>Departments of Neuropediatrics and Neurosurgery, National Neurological Institute “C. Besta,” Milan, Italy</json:string></affiliations></json:item><json:item><name>Chiara Conti MD</name><affiliations><json:string>Departments of Neuropediatrics and Neurosurgery, National Neurological Institute “C. Besta,” Milan, Italy</json:string></affiliations></json:item><json:item><name>Ivano Dones MD</name><affiliations><json:string>Department of Neurosurgery, National Neurological Institute “C. Besta,” Milan, Italy</json:string></affiliations></json:item><json:item><name>Giovanni Broggi MD</name><affiliations><json:string>Department of Neurosurgery, National Neurological Institute “C. Besta,” Milan, Italy</json:string></affiliations></json:item></author><subject><json:item><lang><json:string>eng</json:string></lang><value>Deep brain stimulation</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>Pallidal stimulation</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>Refractory dystonia</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>Refractory dyskinesia</value></json:item></subject><language><json:string>eng</json:string></language><abstract>We report a 13‐year‐old boy who developed severe, refractory dystonia–dyskinesias as an abrupt worsening of a previously nonprogressive movement disorder. The movements became continuous, requiring artificial respiration and continuous sedation in the intensive‐care unit. Various drugs and drug combinations failed to achieve control. The child was then treated successfully with bilateral pallidal (GPi) stimulation as shown in the videotape. Four months later and without medication, the boy regained autonomous gait and audible speech; his neurologic condition continues to improve.</abstract><qualityIndicators><score>2.384</score><pdfVersion>1.3</pdfVersion><pdfPageSize>612 x 792 pts (letter)</pdfPageSize><refBibsNative>true</refBibsNative><abstractCharCount>586</abstractCharCount><pdfWordCount>1436</pdfWordCount><pdfCharCount>9815</pdfCharCount><pdfPageCount>3</pdfPageCount><abstractWordCount>79</abstractWordCount></qualityIndicators><title>Life‐threatening dystonia–dyskinesias in a child: Successful treatment with bilateral pallidal stimulation</title><genre><json:string>Serial article</json:string></genre><host><volume>15</volume><pages><total>3</total><last>1012</last><first>1010</first></pages><issn><json:string>0885-3185</json:string></issn><issue>5</issue><subject><json:item><value>Brief Report</value></json:item></subject><genre></genre><language><json:string>unknown</json:string></language><title>Movement Disorders</title><doi><json:string>10.1002/(ISSN)1531-8257</json:string></doi></host><publicationDate>2000</publicationDate><copyrightDate>2000</copyrightDate><doi><json:string>10.1002/1531-8257(200009)15:5>1010::AID-MDS1039>3.0.CO;2-5</json:string></doi><id>E6182ED5DFEB2ABD4405F44F80898F66B7D3B038</id><fulltext><json:item><original>true</original><mimetype>application/pdf</mimetype><extension>pdf</extension><uri>https://api.istex.fr/document/E6182ED5DFEB2ABD4405F44F80898F66B7D3B038/fulltext/pdf</uri></json:item><json:item><original>false</original><mimetype>application/zip</mimetype><extension>zip</extension><uri>https://api.istex.fr/document/E6182ED5DFEB2ABD4405F44F80898F66B7D3B038/fulltext/zip</uri></json:item><istex:fulltextTEI uri="https://api.istex.fr/document/E6182ED5DFEB2ABD4405F44F80898F66B7D3B038/fulltext/tei"><teiHeader type="text"><fileDesc><titleStmt><title level="a" type="main" xml:lang="en">Life‐threatening dystonia–dyskinesias in a child: Successful treatment with bilateral pallidal stimulation</title></titleStmt><publicationStmt><authority>ISTEX</authority><publisher>John Wiley & Sons, Inc.</publisher><pubPlace>New York</pubPlace><availability><p>John Wiley & Sons, Inc.</p></availability><date>2000</date></publicationStmt><sourceDesc><biblStruct type="inbook"><analytic><title level="a" type="main" xml:lang="en">Life‐threatening dystonia–dyskinesias in a child: Successful treatment with bilateral pallidal stimulation</title><author><persName><forename type="first">Lucia</forename><surname>Angelini</surname><roleName type="degree">MD</roleName></persName><note type="correspondence"><p>Correspondence: Department of Neuropediatrics, National Neurological Institute “C. Besta,” Via Celoria 11, 20133 Milan, Italy</p></note><affiliation>Departments of Neuropediatrics and Neurosurgery, National Neurological Institute “C. Besta,” Milan, Italy</affiliation></author><author><persName><forename type="first">Nardo</forename><surname>Nardocci</surname><roleName type="degree">MD</roleName></persName><affiliation>Departments of Neuropediatrics and Neurosurgery, National Neurological Institute “C. Besta,” Milan, Italy</affiliation></author><author><persName><forename type="first">Margherita</forename><surname>Estienne</surname><roleName type="degree">MD</roleName></persName><affiliation>Departments of Neuropediatrics and Neurosurgery, National Neurological Institute “C. Besta,” Milan, Italy</affiliation></author><author><persName><forename type="first">Chiara</forename><surname>Conti</surname><roleName type="degree">MD</roleName></persName><affiliation>Departments of Neuropediatrics and Neurosurgery, National Neurological Institute “C. Besta,” Milan, Italy</affiliation></author><author><persName><forename type="first">Ivano</forename><surname>Dones</surname><roleName type="degree">MD</roleName></persName><affiliation>Department of Neurosurgery, National Neurological Institute “C. Besta,” Milan, Italy</affiliation></author><author><persName><forename type="first">Giovanni</forename><surname>Broggi</surname><roleName type="degree">MD</roleName></persName><affiliation>Department of Neurosurgery, National Neurological Institute “C. Besta,” Milan, Italy</affiliation></author></analytic><monogr><title level="j">Movement Disorders</title><title level="j" type="abbrev">Mov. Disord.</title><idno type="pISSN">0885-3185</idno><idno type="eISSN">1531-8257</idno><idno type="DOI">10.1002/(ISSN)1531-8257</idno><imprint><publisher>John Wiley & Sons, Inc.</publisher><pubPlace>New York</pubPlace><date type="published" when="2000-09"></date><biblScope unit="vol">15</biblScope><biblScope unit="issue">5</biblScope><biblScope unit="page" from="1010">1010</biblScope><biblScope unit="page" to="1012">1012</biblScope></imprint></monogr><idno type="istex">E6182ED5DFEB2ABD4405F44F80898F66B7D3B038</idno><idno type="DOI">10.1002/1531-8257(200009)15:5<1010::AID-MDS1039>3.0.CO;2-5</idno><idno type="ArticleID">MDS1039</idno></biblStruct></sourceDesc></fileDesc><profileDesc><creation><date>2000</date></creation><langUsage><language ident="en">en</language></langUsage><abstract xml:lang="en"><p>We report a 13‐year‐old boy who developed severe, refractory dystonia–dyskinesias as an abrupt worsening of a previously nonprogressive movement disorder. The movements became continuous, requiring artificial respiration and continuous sedation in the intensive‐care unit. Various drugs and drug combinations failed to achieve control. The child was then treated successfully with bilateral pallidal (GPi) stimulation as shown in the videotape. Four months later and without medication, the boy regained autonomous gait and audible speech; his neurologic condition continues to improve.</p></abstract><textClass xml:lang="en"><keywords scheme="keyword"><list><head>Keywords</head><item><term>Deep brain stimulation</term></item><item><term>Pallidal stimulation</term></item><item><term>Refractory dystonia</term></item><item><term>Refractory dyskinesia</term></item></list></keywords></textClass><textClass><keywords scheme="Journal Subject"><list><head>Article category</head><item><term>Brief Report</term></item></list></keywords></textClass></profileDesc><revisionDesc><change when="1999-07-12">Received</change><change when="2000-04-04">Registration</change><change when="2000-09">Published</change></revisionDesc></teiHeader></istex:fulltextTEI><json:item><original>false</original><mimetype>text/plain</mimetype><extension>txt</extension><uri>https://api.istex.fr/document/E6182ED5DFEB2ABD4405F44F80898F66B7D3B038/fulltext/txt</uri></json:item></fulltext><metadata><istex:metadataXml wicri:clean="Wiley, elements deleted: body"><istex:xmlDeclaration>version="1.0" encoding="UTF-8" standalone="yes"</istex:xmlDeclaration><istex:document><component version="2.0" type="serialArticle" xml:lang="en"><header><publicationMeta level="product"><publisherInfo><publisherName>John Wiley & Sons, Inc.</publisherName><publisherLoc>New York</publisherLoc></publisherInfo><doi registered="yes">10.1002/(ISSN)1531-8257</doi><issn type="print">0885-3185</issn><issn type="electronic">1531-8257</issn><idGroup><id type="product" value="MDS"></id></idGroup><titleGroup><title type="main" xml:lang="en" sort="MOVEMENT DISORDERS">Movement Disorders</title><title type="short">Mov. Disord.</title></titleGroup></publicationMeta><publicationMeta level="part" position="50"><doi origin="wiley" registered="yes">10.1002/1531-8257(200009)15:5<>1.0.CO;2-S</doi><numberingGroup><numbering type="journalVolume" number="15">15</numbering><numbering type="journalIssue">5</numbering></numberingGroup><coverDate startDate="2000-09">September 2000</coverDate></publicationMeta><publicationMeta level="unit" type="shortCommunication" position="39" status="forIssue"><doi origin="wiley" registered="yes">10.1002/1531-8257(200009)15:5<1010::AID-MDS1039>3.0.CO;2-5</doi><idGroup><id type="unit" value="MDS1039"></id></idGroup><countGroup><count type="pageTotal" number="3"></count></countGroup><titleGroup><title type="articleCategory">Brief Report</title><title type="tocHeading1">Brief Reports</title></titleGroup><copyright ownership="thirdParty">Copyright © 2000 Movement Disorder Society</copyright><eventGroup><event type="manuscriptReceived" date="1999-07-12"></event><event type="manuscriptRevised" date="1999-10-06"></event><event type="manuscriptAccepted" date="2000-04-04"></event><event type="firstOnline" date="2001-01-23"></event><event type="publishedOnlineFinalForm" date="2001-01-23"></event><event type="xmlConverted" agent="Converter:JWSART34_TO_WML3G version:2.3.18.1 mode:FullText source:HeaderRef result:HeaderRef" date="2010-09-09"></event><event type="xmlConverted" agent="Converter:WILEY_ML3G_TO_WILEY_ML3GV2 version:3.8.8" date="2014-02-02"></event><event type="xmlConverted" agent="Converter:WML3G_To_WML3G version:4.1.7 mode:FullText,remove_FC" date="2014-10-31"></event></eventGroup><numberingGroup><numbering type="pageFirst">1010</numbering><numbering type="pageLast">1012</numbering></numberingGroup><correspondenceTo>Department of Neuropediatrics, National Neurological Institute “C. Besta,” Via Celoria 11, 20133 Milan, Italy</correspondenceTo><linkGroup><link type="toTypesetVersion" href="file:MDS.MDS1039.pdf"></link></linkGroup></publicationMeta><contentMeta><countGroup><count type="figureTotal" number="0"></count><count type="tableTotal" number="0"></count><count type="referenceTotal" number="9"></count><count type="wordTotal" number="1396"></count></countGroup><titleGroup><title type="main" xml:lang="en">Life‐threatening dystonia–dyskinesias in a child: Successful treatment with bilateral pallidal stimulation</title><title type="short" xml:lang="en">Pallidal Stimulation in Intractable Dystonia</title></titleGroup><creators><creator xml:id="au1" creatorRole="author" affiliationRef="#af1" corresponding="yes"><personName><givenNames>Lucia</givenNames><familyName>Angelini</familyName><degrees>MD</degrees></personName></creator><creator xml:id="au2" creatorRole="author" affiliationRef="#af1"><personName><givenNames>Nardo</givenNames><familyName>Nardocci</familyName><degrees>MD</degrees></personName></creator><creator xml:id="au3" creatorRole="author" affiliationRef="#af1"><personName><givenNames>Margherita</givenNames><familyName>Estienne</familyName><degrees>MD</degrees></personName></creator><creator xml:id="au4" creatorRole="author" affiliationRef="#af1"><personName><givenNames>Chiara</givenNames><familyName>Conti</familyName><degrees>MD</degrees></personName></creator><creator xml:id="au5" creatorRole="author" affiliationRef="#af2"><personName><givenNames>Ivano</givenNames><familyName>Dones</familyName><degrees>MD</degrees></personName></creator><creator xml:id="au6" creatorRole="author" affiliationRef="#af2"><personName><givenNames>Giovanni</givenNames><familyName>Broggi</familyName><degrees>MD</degrees></personName></creator></creators><affiliationGroup><affiliation xml:id="af1" countryCode="IT" type="organization"><unparsedAffiliation>Departments of Neuropediatrics and Neurosurgery, National Neurological Institute “C. Besta,” Milan, Italy</unparsedAffiliation></affiliation><affiliation xml:id="af2" countryCode="IT" type="organization"><unparsedAffiliation>Department of Neurosurgery, National Neurological Institute “C. Besta,” Milan, Italy</unparsedAffiliation></affiliation></affiliationGroup><keywordGroup xml:lang="en" type="author"><keyword xml:id="kwd1">Deep brain stimulation</keyword><keyword xml:id="kwd2">Pallidal stimulation</keyword><keyword xml:id="kwd3">Refractory dystonia</keyword><keyword xml:id="kwd4">Refractory dyskinesia</keyword></keywordGroup><abstractGroup><abstract type="main" xml:lang="en"><title type="main">Abstract</title><p>We report a 13‐year‐old boy who developed severe, refractory dystonia–dyskinesias as an abrupt worsening of a previously nonprogressive movement disorder. The movements became continuous, requiring artificial respiration and continuous sedation in the intensive‐care unit. Various drugs and drug combinations failed to achieve control. The child was then treated successfully with bilateral pallidal (GPi) stimulation as shown in the videotape. Four months later and without medication, the boy regained autonomous gait and audible speech; his neurologic condition continues to improve.</p></abstract></abstractGroup></contentMeta></header></component></istex:document></istex:metadataXml><!--Version 0.6 générée le 3-12-2015--><mods version="3.6"><titleInfo lang="en"><title>Life‐threatening dystonia–dyskinesias in a child: Successful treatment with bilateral pallidal stimulation</title></titleInfo><titleInfo type="abbreviated" lang="en"><title>Pallidal Stimulation in Intractable Dystonia</title></titleInfo><titleInfo type="alternative" contentType="CDATA" lang="en"><title>Life‐threatening dystonia–dyskinesias in a child: Successful treatment with bilateral pallidal stimulation</title></titleInfo><name type="personal"><namePart type="given">Lucia</namePart><namePart type="family">Angelini</namePart><namePart type="termsOfAddress">MD</namePart><affiliation>Departments of Neuropediatrics and Neurosurgery, National Neurological Institute “C. Besta,” Milan, Italy</affiliation><description>Correspondence: Department of Neuropediatrics, National Neurological Institute “C. Besta,” Via Celoria 11, 20133 Milan, Italy</description><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Nardo</namePart><namePart type="family">Nardocci</namePart><namePart type="termsOfAddress">MD</namePart><affiliation>Departments of Neuropediatrics and Neurosurgery, National Neurological Institute “C. Besta,” Milan, Italy</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Margherita</namePart><namePart type="family">Estienne</namePart><namePart type="termsOfAddress">MD</namePart><affiliation>Departments of Neuropediatrics and Neurosurgery, National Neurological Institute “C. Besta,” Milan, Italy</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Chiara</namePart><namePart type="family">Conti</namePart><namePart type="termsOfAddress">MD</namePart><affiliation>Departments of Neuropediatrics and Neurosurgery, National Neurological Institute “C. Besta,” Milan, Italy</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Ivano</namePart><namePart type="family">Dones</namePart><namePart type="termsOfAddress">MD</namePart><affiliation>Department of Neurosurgery, National Neurological Institute “C. Besta,” Milan, Italy</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Giovanni</namePart><namePart type="family">Broggi</namePart><namePart type="termsOfAddress">MD</namePart><affiliation>Department of Neurosurgery, National Neurological Institute “C. Besta,” Milan, Italy</affiliation><role><roleTerm type="text">author</roleTerm></role></name><typeOfResource>text</typeOfResource><genre authority="originalCategForm">shortCommunication</genre><originInfo><publisher>John Wiley & Sons, Inc.</publisher><place><placeTerm type="text">New York</placeTerm></place><dateIssued encoding="w3cdtf">2000-09</dateIssued><dateCaptured encoding="w3cdtf">1999-07-12</dateCaptured><dateValid encoding="w3cdtf">2000-04-04</dateValid><copyrightDate encoding="w3cdtf">2000</copyrightDate></originInfo><language><languageTerm type="code" authority="rfc3066">en</languageTerm><languageTerm type="code" authority="iso639-2b">eng</languageTerm></language><physicalDescription><internetMediaType>text/html</internetMediaType><extent unit="references">9</extent><extent unit="words">1396</extent></physicalDescription><abstract lang="en">We report a 13‐year‐old boy who developed severe, refractory dystonia–dyskinesias as an abrupt worsening of a previously nonprogressive movement disorder. The movements became continuous, requiring artificial respiration and continuous sedation in the intensive‐care unit. Various drugs and drug combinations failed to achieve control. The child was then treated successfully with bilateral pallidal (GPi) stimulation as shown in the videotape. Four months later and without medication, the boy regained autonomous gait and audible speech; his neurologic condition continues to improve.</abstract><subject lang="en"><genre>Keywords</genre><topic>Deep brain stimulation</topic><topic>Pallidal stimulation</topic><topic>Refractory dystonia</topic><topic>Refractory dyskinesia</topic></subject><relatedItem type="host"><titleInfo><title>Movement Disorders</title></titleInfo><titleInfo type="abbreviated"><title>Mov. Disord.</title></titleInfo><subject><genre>article category</genre><topic>Brief Report</topic></subject><identifier type="ISSN">0885-3185</identifier><identifier type="eISSN">1531-8257</identifier><identifier type="DOI">10.1002/(ISSN)1531-8257</identifier><identifier type="PublisherID">MDS</identifier><part><date>2000</date><detail type="volume"><caption>vol.</caption><number>15</number></detail><detail type="issue"><caption>no.</caption><number>5</number></detail><extent unit="pages"><start>1010</start><end>1012</end><total>3</total></extent></part></relatedItem><identifier type="istex">E6182ED5DFEB2ABD4405F44F80898F66B7D3B038</identifier><identifier type="DOI">10.1002/1531-8257(200009)15:5<1010::AID-MDS1039>3.0.CO;2-5</identifier><identifier type="ArticleID">MDS1039</identifier><accessCondition type="use and reproduction" contentType="copyright">Copyright © 2000 Movement Disorder Society</accessCondition><recordInfo><recordOrigin>John Wiley & Sons, Inc.</recordOrigin><recordContentSource>WILEY</recordContentSource></recordInfo></mods></metadata><serie></serie></istex></record>Pour manipuler ce document sous Unix (Dilib)
EXPLOR_STEP=$WICRI_ROOT/Wicri/Santé/explor/MovDisordV3/Data/Istex/Corpus
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 003947 | SxmlIndent | more
Ou
HfdSelect -h $EXPLOR_AREA/Data/Istex/Corpus/biblio.hfd -nk 003947 | SxmlIndent | more
Pour mettre un lien sur cette page dans le réseau Wicri
{{Explor lien
|wiki= Wicri/Santé
|area= MovDisordV3
|flux= Istex
|étape= Corpus
|type= RBID
|clé= ISTEX:E6182ED5DFEB2ABD4405F44F80898F66B7D3B038
|texte= Life‐threatening dystonia–dyskinesias in a child: Successful treatment with bilateral pallidal stimulation
}}
| This area was generated with Dilib version V0.6.23. |  |