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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-10-70-a</article-id>
<article-id pub-id-type="doi">10.15844/pedneurbriefs-10-9-9</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Endocrine Disorders and Cognition</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>Thyroxine-Induced Absences in JME</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>09</month>
<year>1996</year>
</pub-date>
<pub-date date-type="pub" publication-format="electronic">
<day>01</day>
<month>06</month>
<year>2016</year>
</pub-date>
<volume>10</volume>
<issue>9</issue>
<fpage>70</fpage>
<lpage>70</lpage>
<permissions>
<copyright-statement>Copyright: &#x00A9; 1996 The Author(s)</copyright-statement>
<copyright-year>1996</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="10.1212/WNL.47.2.605-a" vol="47" page="605">
<article-title>Thyroxine exacerbates absence seizures in juvenile myoclonic epilepsy</article-title>
</related-article>
<abstract abstract-type="web-summary" specific-use="electronic-only">
<p>A patient with juvenile myoclonic epilepsy (JME), manifested as absences at age 10 and myoclonic jerking and generalized tonic clonic seizures at age 15, was treated successfully with primidone at the King Fahad National Guard Hospital, Riyadh, Saudi Arabia.</p>
</abstract>
<kwd-group>
<kwd>Juvenile Myoclonic Epilepsy</kwd>
<kwd>Tonic Clonic Seizures</kwd>
<kwd>Multispike</kwd>
</kwd-group>
</article-meta>
</front>
<body>
<p>A patient with juvenile myoclonic epilepsy (JME), manifested as absences at age 10 and myoclonic jerking and generalized tonic clonic seizures at age 15, was treated successfully with primidone at the King Fahad National Guard Hospital, Riyadh, Saudi Arabia. Absence seizures were provoked by thyroxine 50 mcg daily prescribed at age 35 for a simple goitre associated with normal thyroid function tests. Loss of concentration lasting a few seconds was associated with frequent discharges of sharp, spike, multispike, and slow wave complexes on the EEG. The thyroid levels were slightly elevated compared to initial tests. Absences stopped and the EEG returned to normal after thyroxine was discontinued. [<xref ref-type="bibr" rid="CIT0001">1</xref>]</p>
<p>COMMENT. When thyroid hormone is administered in patients with epilepsy, the dose should be monitored carefully and an EEG obtained to examine for subclinical absence seizures requiring additional antiepileptic medication.</p>
</body>
<back>
<ref-list>
<ref id="CIT0001">
<label>1</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Obeid</surname>
<given-names>T</given-names>
</name>
<name>
<surname>Awada</surname>
<given-names>A</given-names>
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<article-title>Thyroxine exacerbates absence seizures in juvenile myoclonic epilepsy</article-title>
<source>Neurology</source>
<year>1996</year>
<month>Aug</month>
<volume>47</volume>
<issue>2</issue>
<fpage>605</fpage>
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<pub-id pub-id-type="pmid">8757055</pub-id>
<pub-id pub-id-type="doi">10.1212/WNL.47.2.605-a</pub-id>
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</ref-list>
</back>
</article>
