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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-5-50-a</article-id>
<article-id pub-id-type="doi">10.15844/pedneurbriefs-5-7-2</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Behavior and Learning 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>Organic Brain Dysfunction and Autism</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>1991</year>
</pub-date>
<pub-date date-type="pub" publication-format="electronic">
<day>01</day>
<month>07</month>
<year>2016</year>
</pub-date>
<volume>5</volume>
<issue>7</issue>
<fpage>50</fpage>
<lpage>50</lpage>
<permissions>
<copyright-statement>Copyright: &#x00A9; 1991 The Author(s)</copyright-statement>
<copyright-year>1991</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.1469-8749.1991.tb14915.x" vol="33" page="495">
<article-title>Neuropsychiatric assessment of children with autism: a population-based study</article-title>
</related-article>
<abstract abstract-type="web-summary" specific-use="electronic-only">
<p>A population-based neurobiological study of 35 children with autistic disorder (AD) and 17 with autistic-like conditions (ALC) is reported from the Department of Child and Adolescent Psychiatry, University of Goteborg, Sweden.</p>
</abstract>
<kwd-group>
<kwd>Autistic Disorder</kwd>
<kwd>Moebius Syndrome</kwd>
<kwd>Brain Damage</kwd>
</kwd-group>
</article-meta>
</front>
<body>
<p>A population-based neurobiological study of 35 children with autistic disorder (AD) and 17 with autistic-like conditions (ALC) is reported from the Department of Child and Adolescent Psychiatry, University of Goteborg, Sweden. Major indications of brain damage or dysfunction were found in 90%. Etiological groups included Moebius syndrome (9%), fragile X syndrome (6%), chromosomal anomalies (6%), neurocutaneous disorders (6%), congenital hydrocephalus (3%), Rett syndrome (3%), Laurence-Moon-Biedl syndrome (3%), severe perinatal distress (9%), and epilepsy or severe EEG pathology (20%). Genetic factors were implicated in 9% with fathers and a brother with Asperger&#x2019;s syndrome. The EEG was abnormal in 50% and 18 (40%) had epileptiform discharges, maximal in the temporal lobes. CAT scan abnormalities in 25% included dilated ventricles, porencephaly, and general atrophy. BAERs were abnormal in 33%. [<xref ref-type="bibr" rid="CIT0001">1</xref>]</p>
<disp-quote>
<p><bold>COMMENT.</bold> Multiple biological etiologies for autism and autistic-like disorders are suggested by this comprehensive study. Despite the extra effort and patience involved, the pediatric neurologist should not dismiss the child with autistic symptoms to the care of the psychiatrist without first attempting a full neurologic evaluation including EEG and CT or MRI.</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>Steffenburg</surname>
<given-names>S</given-names>
</name>
</person-group>
<article-title>Neuropsychiatric assessment of children with autism: a population-based study</article-title>
<source>Dev Med Child Neurol</source>
<year>1991</year>
<month>Jun</month>
<volume>33</volume>
<issue>6</issue>
<fpage>495</fpage>
<lpage>511</lpage>
<pub-id pub-id-type="doi">10.1111/j.1469-8749.1991.tb14915.x</pub-id>
<pub-id pub-id-type="pmid">1864476</pub-id>
</element-citation>
</ref>
</ref-list>
</back>
</article>