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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-7-07-a</article-id>
<article-id pub-id-type="doi">10.15844/pedneurbriefs-7-1-11</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Encephalopathies</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>Acute Encephalopathy of Obscure Origin</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>1993</year>
</pub-date>
<pub-date date-type="pub" publication-format="electronic">
<day>01</day>
<month>07</month>
<year>2016</year>
</pub-date>
<volume>7</volume>
<issue>1</issue>
<fpage>7</fpage>
<lpage>7</lpage>
<permissions>
<copyright-statement>Copyright: &#x00A9; 1993 The Author(s)</copyright-statement>
<copyright-year>1993</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/S0022-3476(05)80326-9" vol="121" page="845">
<article-title>Coma associated with intense bursts of abnormal movements and long-lasting cognitive disturbances: an acute encephalopathy of obscure origin</article-title>
</related-article>
<abstract abstract-type="web-summary" specific-use="electronic-only">
<p>Six previously healthy children who developed an acute encephalopathy several days after a prodromal illness are reported from the Hopital Bicetre, and Hopital Necker-Enfants Malades, Paris, France.</p>
</abstract>
<kwd-group>
<kwd>Acute Encephalo-Pathy Several</kwd>
<kwd>Prodromal Illnesses</kwd>
<kwd>Orofacial Dyskinesia</kwd>
</kwd-group>
</article-meta>
</front>
<body>
<p>Six previously healthy children who developed an acute encephalopathy several days after a prodromal illness are reported from the Hopital Bicetre, and Hopital Necker-Enfants Malades, Paris, France. Prodromal illnesses consisted of upper respiratory infection with fever, and headache and vomiting. Coma was the initial symptom in 4 patients. Abnormal movements included gesticulation, chewing, swallowing, orofacial dyskinesia, limb dystonia, and choreoathetosis. Rigidity was constant in 5 patients and intermittent in one. Seizures occurred in 2 patients. Recovery extended for several weeks and was characterized by a rapid return of motor function and persistent behavioral and cognitive disturbances. Four patients recovered fully, and two had mild sequelae. [<xref ref-type="bibr" rid="CIT0001">1</xref>]</p>
<disp-quote>
<p><bold>COMMENT.</bold> These cases with a favorable outcome were thought to represent a different syndrome from that described by Lyon, Dodge, and Adams, whose 16 patients died from an acute encephalopathy of obscure origin. Attempts at viral isolation and antibody detection were negative.</p>
</disp-quote>
</body>
<back>
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