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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-2012-26-10-10</article-id>
<article-id pub-id-type="doi">10.15844/pedneurbriefs-26-10-10</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Movement 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 Clinical Course of Tourette 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, Ann &#x0026; Robert H. Lurie Children&#x0027;s Hospital of Chicago, 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>10</month>
<year>2012</year>
</pub-date>
<pub-date date-type="pub" publication-format="electronic">
<day>01</day>
<month>11</month>
<year>2015</year>
</pub-date>
<volume>26</volume>
<issue>10</issue>
<fpage>80</fpage>
<lpage>80</lpage>
<permissions>
<copyright-statement>Copyright: &#x00A9; 2012 The Author(s)</copyright-statement>
<copyright-year>2012</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="10.1016/j.braindev.2011.11.006" vol="34" page="667">
<article-title>Long term clinical course of Tourette syndrome</article-title>
</related-article>
<abstract abstract-type="web-summary" specific-use="electronic-only">
<p>Researchers at Catania University, and University Tor Vergata, Rome, Italy studied the course of Tourette syndrome (TS) after 10 years follow-up in 100 children.</p>
</abstract>
<kwd-group>
<kwd>Tourette Syndrome</kwd>
<kwd>Medication</kwd>
<kwd>Severe Prognosis</kwd>
</kwd-group>
</article-meta>
</front>
<body>
<p>Researchers at Catania University, and University Tor Vergata, Rome, Italy studied the course of Tourette syndrome (TS) after 10 years follow-up in 100 children. Of the &#x201C;pure TS&#x201D; group (n=38), 58% were unchanged, whereas 42% changed to TS+OCD phenotype. Of the &#x201C;TS+ADHD&#x201D; group (n=48), 62% changed to pure TS, 35% to TS+OCD, and 2% to TS+ADHD+OCD. Medication was required in 65%. Patients with comorbid condition at onset had a more severe prognosis and lower quality of life scores. [<xref ref-type="bibr" rid="CIT0001">1</xref>]</p>
<p>COMMENT. Patients with pure TS at onset have a favorable prognosis, whereas patients with TS and comorbid disorders, ADHD and OCD, are at risk of impaired quality of life. TS presents with a variety of clinical phenotypes that may change over time. Appropriate treatment of ADHD in children with TS may prevent behavioral problems in adulthood. Comorbidity with ADHD, occurring in 50% of TS patients, causes more disability than motor tics alone [<xref ref-type="bibr" rid="CIT0002">2</xref>]. Children with TS and ADHD have a 32% risk of learning disabilities. [<xref ref-type="bibr" rid="CIT0003">3</xref>]</p>
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