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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-17-40-a</article-id>
<article-id pub-id-type="doi">10.15844/pedneurbriefs-17-5-8</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Neuromuscular 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>Long-Term Outcome in Guillain-Barre 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>05</month>
<year>2003</year>
</pub-date>
<pub-date date-type="pub" publication-format="electronic">
<day>01</day>
<month>03</month>
<year>2016</year>
</pub-date>
<volume>17</volume>
<issue>5</issue>
<fpage>40</fpage>
<lpage>40</lpage>
<permissions>
<copyright-statement>Copyright: &#x00A9; 2003 The Author(s)</copyright-statement>
<copyright-year>2003</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="10.1067/mpd.2003.115" vol="142" page="305">
<article-title>Long-term outcome in children with Guillain-Barr&#x00E9; syndrome</article-title>
</related-article>
<abstract abstract-type="web-summary" specific-use="electronic-only">
<p>The long-term sequelae and early predictors of sequelae were determined in a chart review of 47 children with Guillain-Barre syndrome (GBS) of whom 30 had been treated with intravenous gammaglobulin (IVIG) at The Hospital for Sick Children, Toronto, Canada.</p>
</abstract>
<kwd-group>
<kwd>Guillain-Barre Syndrome</kwd>
<kwd>Intravenous Gammaglobulin</kwd>
<kwd>Long-Term Muscle</kwd>
</kwd-group>
</article-meta>
</front>
<body>
<p>The long-term sequelae and early predictors of sequelae were determined in a chart review of 47 children with Guillain-Barre syndrome (GBS) of whom 30 had been treated with intravenous gammaglobulin (IVIG) at The Hospital for Sick Children, Toronto, Canada. Persisting long-term muscle weakness at least 2 years after recovery was present in 23% of cases. Weakness was mild and patients were functionally independent. Risk factors for long-term muscle weakness were a young age at onset and a rapid progression to maximal weakness in the acute illness (P=0.03). [<xref ref-type="bibr" rid="CIT0001">1</xref>]</p>
<p>COMMENT. Age associated changes in the symptomatology of GBS in children have been reported previously (Sakakihara Y, Kamoshita S. 1991, see <underline>Progress in Poediatric Neurology II</underline>, PNB Publ, 1994;pp271-2). Children between 3 and 9 years are most susceptible, and the total duration of the illness is longer in younger children. Bulbar nerves are most frequently affected in the younger age group, and the facial nerve in older patients. The stage of myelinogenic maturation might explain the age-associated changes in symptomatology of GBS.</p>
</body>
<back>
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<ref id="CIT0001">
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</article>