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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-3-74-a</article-id>
<article-id pub-id-type="doi">10.15844/pedneurbriefs-3-10-2</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Congenital Malformations</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>Agenesis of the Corpus Callosum</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>10</month>
<year>1989</year>
</pub-date>
<pub-date date-type="pub" publication-format="electronic">
<day>01</day>
<month>08</month>
<year>2016</year>
</pub-date>
<volume>3</volume>
<issue>10</issue>
<fpage>74</fpage>
<lpage>74</lpage>
<permissions>
<copyright-statement>Copyright: &#x00A9; 1989 The Author(s)</copyright-statement>
<copyright-year>1989</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="10.1016/0887-8994(89)90088-X" vol="5" page="259">
<article-title>Aicardi syndrome: postmortem findings</article-title>
</related-article>
<abstract abstract-type="web-summary" specific-use="electronic-only">
<p>The postmortem findings in a two month old infant with the typical clinical features of Aicardi syndrome (i.e., infantile spasms, chorioretinal lacunae, and agenesis of the corpus callosum) are reported from the Division of Neurology, Saitama Children&#x2019;s Medical Center, Saitama, Japan.</p>
</abstract>
<kwd-group>
<kwd>Corpus Callosun</kwd>
<kwd>Cortical Heterotropias</kwd>
<kwd>Inmature Neurons</kwd>
</kwd-group>
</article-meta>
</front>
<body>
<p>The postmortem findings in a two month old infant with the typical clinical features of Aicardi syndrome (i.e., infantile spasms, chorioretinal lacunae, and agenesis of the corpus callosum) are reported from the Division of Neurology, Saitama Children&#x2019;s Medical Center, Saitama, Japan. The rostrum of the corpus callosum was absent and the roof of the dilated third ventricle was covered with a thin leptomeningeal membrane. Cortical heterotropias were found adjacent to the anterior horn of the right lateral ventricle and consisted of small immature neurons. The article includes a review of five autopsied patients with this syndrome previously reported in the literature. [<xref ref-type="bibr" rid="CIT0001">1</xref>]</p>
<disp-quote>
<p><underline>COMMENT</underline>. In these cases, a high incidence of EEG laterality and an asymmetry of pathological lesions are of interest. Three of six patients had focal agenesis of the corpus callosum and three had papilloma of the choroid plexus.</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>Hamano</surname>
<given-names>S</given-names>
</name>
<name>
<surname>Yagishita</surname>
<given-names>S</given-names>
</name>
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<article-title>Aicardi syndrome: postmortem findings</article-title>
<source>Pediatr Neurol</source>
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<month>Jul-Aug</month>
<volume>5</volume>
<issue>4</issue>
<fpage>259</fpage>
<lpage>61</lpage>
<pub-id pub-id-type="pmid">2679585</pub-id>
<pub-id pub-id-type="doi">10.1016/0887-8994(89)90088-X</pub-id>
</element-citation>
</ref>
</ref-list>
</back>
</article>
