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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-9-22</article-id>
<article-id pub-id-type="doi">10.15844/pedneurbriefs-9-3-10</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Demyelinating 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>Characteristics of Childhood Multiple Sclerosis</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>03</month>
<year>1995</year>
</pub-date>
<pub-date date-type="pub" publication-format="electronic">
<day>01</day>
<month>06</month>
<year>2016</year>
</pub-date>
<volume>9</volume>
<issue>3</issue>
<fpage>22</fpage>
<lpage>23</lpage>
<permissions>
<copyright-statement>Copyright: &#x00A9; 1995 The Author(s)</copyright-statement>
<copyright-year>1995</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="10.1016/0387-7604(94)00091-B" vol="17" page="9">
<article-title>Pediatric multiple sclerosis report of 14 cases</article-title>
</related-article>
<abstract abstract-type="web-summary" specific-use="electronic-only">
<p>The clinical manfestations of multiple sclerosis (MS) in 14 children are reported from the Universidade de Sao Paulo, Brazil.</p>
</abstract>
<kwd-group>
<kwd>Multiple Sclerosis</kwd>
<kwd>Bladder Dysfunction</kwd>
<kwd>Minor Motor Impairment</kwd>
</kwd-group>
</article-meta>
</front>
<body>
<p>The clinical manfestations of multiple sclerosis (MS) in 14 children are reported from the Universidade de Sao Paulo, Brazil. Age at onset ranged from 2 to 15 years. Initial symptoms varied from minor motor impairment, visual disturbances, bladder dysfunction and paresthesias, to a diffuse encephalopathy, with impaired consciousness. All had a relapsing-remitting course, and one died 6 months after onset with disseminated demyelinating lesions. CT showed demyelination in 6 of 9 patients. MRI showed white matter lesions in the brainstem or cerebral hemispheres in 5 of 6 patients. CSF pleocytosis occurred in 8 of 23 attacks, and g-globulin levels were increased in 7. Visual evoked potentials (VEP) were abnormal in 7 of 8 patients; BAEP in 4 of 8: and SEP in 4 of 8. The importance of paraclinical examinations in diagnosis is emphasized. [<xref ref-type="bibr" rid="CIT0001">1</xref>]</p>
<disp-quote>
<p>COMMENT. The 14 cases were seen in a period of 12 years. Four presented before 5 years of age, and the youngest was 2 years.</p>
<p>According to a report from the George-August University, Gottingen, Germany, published in the review International MS Journal (Hanefeld FA. <underline>Int. MSJ</underline> 1995;1:90-97), 24 cases with MS onset before age 5 years have been published since 1969. In 20 of 39 new patients studied over a 5-year period in Gottingen, the onset was before 10 years. The onset or relapse was preceded by a nonspecific infection, usually an URI, in &#x003E;50%. Of 8 presenting with optic neuritis, 4 developed MS within 2 years. CSF maximal cell count was 900/ml, and protein was increased &#x003E;100 mg%. Oligoclonal bands were absent in one third. VEPs were more frequently abnormal than BAEP and SEP. MRI sometimes showed new lesions without accompanying symptoms or relapse, and remissions were not always reflected in less MRI changes. Patients with juvenile onset (&#x003E;10 years) followed a more severe, frequently relapsing, course than those with onset before puberty.</p>
</disp-quote>
</body>
<back>
<ref-list>
<ref id="CIT0001">
<label>1</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Guilhoto</surname>
<given-names>LM</given-names>
</name>
<name>
<surname>Os&#x00F3;rio</surname>
<given-names>CA</given-names>
</name>
<name>
<surname>Machado</surname>
<given-names>LR</given-names>
</name>
<name>
<surname>de Castro</surname>
<given-names>CP</given-names>
</name>
<name>
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<given-names>ML</given-names>
</name>
<name>
<surname>Callegaro</surname>
<given-names>D</given-names>
</name>
<etal/>
</person-group>
<article-title>Pediatric multiple sclerosis report of 14 cases</article-title>
<source>Brain Dev</source>
<year>1995</year>
<month>Jan-Feb</month>
<volume>17</volume>
<issue>1</issue>
<fpage>9</fpage>
<lpage>12</lpage>
<pub-id pub-id-type="pmid">7762771</pub-id>
<pub-id pub-id-type="doi">10.1016/0387-7604(94)00091-B</pub-id>
</element-citation>
</ref>
</ref-list>
</back>
</article>
