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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-11-03-b</article-id>
<article-id pub-id-type="doi">10.15844/pedneurbriefs-11-1-5</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Seizure 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>Cortical Hypometabolism in West 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>01</month>
<year>1997</year>
</pub-date>
<pub-date date-type="pub" publication-format="electronic">
<day>01</day>
<month>05</month>
<year>2016</year>
</pub-date>
<volume>11</volume>
<issue>1</issue>
<fpage>3</fpage>
<lpage>4</lpage>
<permissions>
<copyright-statement>Copyright: &#x00A9; 1997 The Author(s)</copyright-statement>
<copyright-year>1997</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="10.1111/j.1528-1157.1996.tb00550.x" vol="37" page="1180">
<article-title>Cortical hypometabolism and delayed myelination in West syndrome</article-title>
</related-article>
<abstract abstract-type="web-summary" specific-use="electronic-only">
<p>Serial PET scans and MRIs were performed in 18 infants with West syndrome (WS) to determine the relation between cortical hypometabolism and delayed myelination in a study at Nagoya University School of Medicine, Japan.</p>
</abstract>
<kwd-group>
<kwd>Cortical Hypometabolism</kwd>
<kwd>West Syndrome</kwd>
<kwd>Hypometabolism</kwd>
</kwd-group>
</article-meta>
</front>
<body>
<p>Serial PET scans and MRIs were performed in 18 infants with West syndrome (WS) to determine the relation between cortical hypometabolism and delayed myelination in a study at Nagoya University School of Medicine, Japan. All 8 patients with symptomatic WS showed hypometabolism at onset, with persistence in 5 at 10 months, whereas only 4 of 10 patients with cryptogenic WS showed hypometabolism at onset and none at age 10 months. Localization of EEG abnormalities at 10 months correlated with the region of hypometabolism in only 2. MRI showed delayed myelination in 2 at onset of epilepsy and in 12 at 10 months. Delayed myelination at 10 months was correlated with hypometabolism. [<xref ref-type="bibr" rid="CIT0001">1</xref>]</p>
<p>COMMENT. MRIs repeated at age 10 months may disclose delayed myelination in infants with WS. The delayed myelination is not always explained by ACTH therapy and may reflect the organic brain lesion causing the seizures.</p>
</body>
<back>
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</article>