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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-18-08</article-id>
<article-id pub-id-type="doi">10.15844/pedneurbriefs-18-1-10</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Hereditary Ataxias</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>Febrile Episodic Ataxia with Novel Mutation</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>2004</year>
</pub-date>
<pub-date date-type="pub" publication-format="electronic">
<day>01</day>
<month>03</month>
<year>2016</year>
</pub-date>
<volume>18</volume>
<issue>1</issue>
<fpage>8</fpage>
<lpage>8</lpage>
<permissions>
<copyright-statement>Copyright: &#x00A9; 2004 The Author(s)</copyright-statement>
<copyright-year>2004</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="10.1002/ana.10756" vol="54" page="725">
<article-title>Novel CACNA1A mutation causes febrile episodic ataxia with interictal cerebellar deficits</article-title>
</related-article>
<abstract abstract-type="web-summary" specific-use="electronic-only">
<p>An episodic ataxia type 2 (EA2) kindred with ataxic spells induced by fever or high environmental temperature and a novel <italic>CACNA1A</italic> mutation were identified and reported from the Universities of Mississippi and Minnesota.</p>
</abstract>
<kwd-group>
<kwd>Episodic Ataxia</kwd>
<kwd>Novel CACNA1A Mutation</kwd>
<kwd>Cerebellar Deficits</kwd>
</kwd-group>
</article-meta>
</front>
<body>
<p>An episodic ataxia type 2 (EA2) kindred with ataxic spells induced by fever or high environmental temperature and a novel <italic>CACNA1A</italic> mutation were identified and reported from the Universities of Mississippi and Minnesota. The proband was a 75-year-old woman with episodes beginning in childhood of ataxia, vertigo, weakness, and migraine lasting several hours, and provoked by fever, heat, stress, or sudden movements. The proband&#x2019;s father and sister were similarly affected. In 11 patients with episodic ataxia, age of onset varied from infancy to the twenties. Episodes ranged from daily to 2 annually, and lasted minutes to days. They were sometimes accompanied by headaches, diplopia, nausea, and vertigo. Those with the mutation had interictal cerebellar deficits. Early cerebellar dysfunction in EA2 results from the mutations in the neuronal calcium-channel gene and not a degenerative process. [<xref ref-type="bibr" rid="CIT0001">1</xref>]</p>
<p>COMMENT. Episodic ataxia type 2 (EA2) is a dominantly inherited disorder, characterized by spells of ataxia, dysarthria, vertigo, and migraine, associated with mutations in the neuronal calcium-channel gene CACNA1A. Attacks are precipitated by stress, exercise, or alcohol. Some patients have nystagmus between spells and some develop a progressive ataxia in adulthood. Twenty one CACNA1A mutations have been described in EA2. The above kindred study adds a further mutation and clinical syndrome in which ataxic spells are precipitated by fever or overheating, and patients develop signs of cerebellar dysfunction between attacks. Other neurologic disorders caused by mutations in the CACNA1A gene are the dominantly inherited progressive spinocerebellar ataxia (SCA6), and familial hemiplegic migraine.</p>
</body>
<back>
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<ref id="CIT0001">
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<volume>54</volume>
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<pub-id pub-id-type="doi">10.1002/ana.10756</pub-id>
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</article>