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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-6-53-b</article-id>
<article-id pub-id-type="doi">10.15844/pedneurbriefs-6-7-8</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Cerebrovascular Disease</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>Idiopathic Stroke</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>07</month>
<year>1992</year>
</pub-date>
<pub-date date-type="pub" publication-format="electronic">
<day>01</day>
<month>07</month>
<year>2016</year>
</pub-date>
<volume>6</volume>
<issue>7</issue>
<fpage>53</fpage>
<lpage>54</lpage>
<permissions>
<copyright-statement>Copyright: &#x00A9; 1992 The Author(s)</copyright-statement>
<copyright-year>1992</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="10.1002/ana.410310618" vol="31" page="675">
<article-title>Idiopathic childhood stroke is associated with human leukocyte antigen (HLA)-B51</article-title>
</related-article>
<abstract abstract-type="web-summary" specific-use="electronic-only">
<p>Of 4 children with idiopathic stroke syndrome examined at the Department of Neurosciences and Pediatrics, UMD-New Jersey Medical School and the University of Rochester Medical Center, all 4 were heterozygous for human leukocyte antigen (HLA-B51).</p>
</abstract>
<kwd-group>
<kwd>Human Leukocyte Antigen</kwd>
<kwd>Idiopathic Stroke Syndrome</kwd>
<kwd>Varicella Zoster Virus Infection</kwd>
</kwd-group>
</article-meta>
</front>
<body>
<p>Of 4 children with idiopathic stroke syndrome examined at the Department of Neurosciences and Pediatrics, UMD-New Jersey Medical School and the University of Rochester Medical Center, all 4 were heterozygous for human leukocyte antigen (HLA-B51). Control samples from 3 patients with non-idiopathic stroke syndrome failed to reveal the HAL-B51 marker. [<xref ref-type="bibr" rid="CIT0001">1</xref>]</p>
<disp-quote>
<p><bold>COMMENT.</bold> The finding of a common immunogenetic marker in children with idiopathic stroke syndrome suggests a genetic predisposition and susceptibility. The authors suggest that host factors, possibly triggered by transient viral precipitants, may contribute causally to these vascular occlusions.</p>
<p>Delayed onset hemiparesis and vascular thrombosis may occur approximately 6 weeks after primary varicella zoster virus infection and may explain some cases of misdiagnosed idiopathic stroke in children [<xref ref-type="bibr" rid="CIT0002">2</xref>]. The importance of this clinical entity is emphasized in an editorial (<underline>Lancet</underline> June 13, 1992; <underline>339</underline>:1449-1450). The prognosis was good regardless of therapy and all patients recovered completely or nearly completely. The MRI was more sensitive than CT or angiography in demonstrating infarction of the basal ganglia and/or internal capsule. The delay in onset of the hemiparesis may result from the time taken for the vascular media to be infected with the virus.</p>
</disp-quote>
</body>
<back>
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