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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-1-23</article-id>
<article-id pub-id-type="doi">10.15844/pedneurbriefs-1-4-1</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>Immunogenetic Aspects of Febrile Convulsions</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>1987</year>
</pub-date>
<pub-date date-type="pub" publication-format="electronic">
<day>01</day>
<month>08</month>
<year>2016</year>
</pub-date>
<volume>1</volume>
<issue>4</issue>
<fpage>23</fpage>
<lpage>24</lpage>
<permissions>
<copyright-statement>Copyright: &#x00A9; 1987 The Author(s)</copyright-statement>
<copyright-year>1987</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="10.3109/01677068709102347" vol="4" page="267">
<article-title>Immunogenetic aspects of febrile convulsions</article-title>
</related-article>
<abstract abstract-type="web-summary" specific-use="electronic-only">
<p>Investigators in Genetics, Pediatrics, Neurology, and Immunology, at Mansoura Un., Mansoura, Egypt found a gene frequency of 0.284 (c.f.</p>
</abstract>
<kwd-group>
<kwd>Febrile Convulsions</kwd>
<kwd>HLA-B5 Antigen</kwd>
<kwd>Genetic Control</kwd>
</kwd-group>
</article-meta>
</front>
<body>
<p>Investigators in Genetics, Pediatrics, Neurology, and Immunology, at Mansoura Un., Mansoura, Egypt found a gene frequency of 0.284 (c.f. 0.093 in controls) and a highly significant association between HLA-B5 antigen and febrile convulsions in 39 patients compared to 380 healthy controls. The high frequency of HLA-B5 antigen (48.7 in patients c.f., 17.6 in controls) reflected a significantly high relative risk and indicated that children having antigen B5 are 4.4 times more susceptible to febrile convulsions than those without that antigen. The means of IgA (89 mg%) and E-rosette (54%) were significantly <underline>low</underline> c.f. controls (151 and 64, respectively). The authors suggest that the genetic control of febrile convulsions is in linkage disequilibrium with HLA-B5, low IgA and low total T-cells and that this altered immune function may predispose to acute infections and high fever which precipitate the febrile convulsions. [<xref ref-type="bibr" rid="CIT0001">1</xref>]</p>
<disp-quote>
<p><bold><underline>COMMENT</underline>:</bold> Ehrengut W and Ehrengut J [<xref ref-type="bibr" rid="CIT0002">2</xref>] found a lack of immunoglobulins beta-2A and beta-2M and a reduction of gamma globulin in 4 of 6 patients and postulated a weakness of defense mechanisms against infection as a possible cause of febrile convulsions. This report was the first and only reference to hypoimmunoglobulinemia cited in the monograph <underline>Febrile Convulsions</underline> 1968 MacMillan, N.Y., which included a review of world literature published in English and foreign languages. Isaac et al [<xref ref-type="bibr" rid="CIT0003">3</xref>] reported low serum IgA in children with febrile convulsions and Grob and Herold [<xref ref-type="bibr" rid="CIT0004">4</xref>] and others have found IgA deficiency among epileptics receiving anticonvulsants, especially hydantoins (see Hafez et al).</p>
<p>The multifactorial inheritance of febrile seizures is alluded to in the 6th annual Merritt-Putnam Symposium [<xref ref-type="bibr" rid="CIT0005">5</xref>]. Siblings have approximately a 8-12% risk of alio having febrile seizures. If the index child and one parent are affected, the risks to siblings are 30-40% (50% if both parents are affected). A high proportion of probands and their siblings develop EEG abnormalities 3-5 years after the febrile seizure, including generalized spike-and-wave and a photoconvulsive response (Hauser et al 1985; Millichap, 1968).</p>
</disp-quote>
</body>
<back>
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