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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-16-94</article-id>
<article-id pub-id-type="doi">10.15844/pedneurbriefs-16-12-9</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Periodic Syndromes</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>Kleine-Levin Syndrome: An Autoimmune Hypothesis</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>12</month>
<year>2002</year>
</pub-date>
<pub-date date-type="pub" publication-format="electronic">
<day>01</day>
<month>04</month>
<year>2016</year>
</pub-date>
<volume>16</volume>
<issue>12</issue>
<fpage>94</fpage>
<lpage>95</lpage>
<permissions>
<copyright-statement>Copyright: &#x00A9; 2002 The Author(s)</copyright-statement>
<copyright-year>2002</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="10.1212/01.WNL.0000036605.89977.D0" vol="59" page="1739">
<article-title>Kleine-Levin syndrome: an autoimmune hypothesis based on clinical and genetic analyses</article-title>
</related-article>
<abstract abstract-type="web-summary" specific-use="electronic-only">
<p>Clinical, polysomnographic, CSF, CT, and MRI records and genotype data of 30 unrelated patients with Kleine-Levin syndrome (KLS) and their families were studied at Hopital Gui-de-Chauliac, Montpellier, France, and other sleep centers.</p>
</abstract>
<kwd-group>
<kwd>Kleine-Levin Syndrome</kwd>
<kwd>Autoimmune Etiology</kwd>
<kwd>Human Leukocyte Antigen</kwd>
</kwd-group>
</article-meta>
</front>
<body>
<p>Clinical, polysomnographic, CSF, CT, and MRI records and genotype data of 30 unrelated patients with Kleine-Levin syndrome (KLS) and their families were studied at Hopital Gui-de-Chauliac, Montpellier, France, and other sleep centers. The sex ratio showed a predominance of males (25/5). The mean age at onset was 15 +/- 3 years. The mean number of episodes per year was 4 +/- 3 and the mean duration of episodes was 12 +/- 8 days. Viral upper respiratory tract infection was a precipitating factor in 16/23 (70%). The two essential diagnostic criteria, recurrent hypersomnia with asssociated cognitive and mood disturbances, were present in all patients. Hyperphagia occurred in 17 (57%), and hypersexuality in 14 (47%) patients. Brain imaging and CSF were normal. EEGs were not recorded. Treatment for hypersomnia that was partially effective included the stimulant, modafinil, carbamazepine, and lithium. Neuroleptics were ineffective. The genotype data analysis of KLS patients, contrasted with normal controls, found a significant increase in the frequency of human leukocyte antigen (HLA)-DQB1*0201 allele, and 3 patients with KLS were homozygous for DQB1*0201, 2 from the same family. An autoimmune etiology is suggested. [<xref ref-type="bibr" rid="CIT0001">1</xref>]</p>
<p>COMMENT. The etiology of Kleine-Levin syndrome is unknown. Periodic hypothalamic dysfunction, focal encephalitis, and an autoimmune process are possibilities. The disorder is rarely familial, only in 2 of 30 patients in the above study, and in 2 siblings in the following report. Levels of CSF orexin (hypocretin), decreased in some narcoleptic patients, were normal in the following familial cases.</p>
<p><bold>Familial Kleine-Levin syndrome</bold> is reported in 2 siblings with unusually long hypersomnic spells, from Tufts University, Boston, MA [<xref ref-type="bibr" rid="CIT0002">2</xref>]. Both patients shared the HLA-DR2, DQ1, and DR5 haplotypes. Treatment with lithium, methylphenidate, modafinil, clonazepam, and other drugs was ineffective in preventing or reducing the duration of hypersomnic spells. Patient 1, a 15-year-old boy, developed flu-like symptoms without fever, he slept excessively for 9 days, and was irritable when awake. Eight similar attacks occurred during the following 10 months, and 16 hypersomnic spells in 5 years. Compulsive symptoms followed the episodes. Patient 2, the sister of patient 1, began having hypersomnic spells at age 13 years, the first preceded by a flu-like illness. Between attacks, MRI, EEG, Ebstein-Barr virus titer, ESR, and CSF were normal.</p>
</body>
<back>
<ref-list>
<ref id="CIT0001">
<label>1</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Dauvilliers</surname>
<given-names>Y</given-names>
</name>
<name>
<surname>Mayer</surname>
<given-names>G</given-names>
</name>
<name>
<surname>Lecendreux</surname>
<given-names>M</given-names>
</name>
<name>
<surname>Neidhart</surname>
<given-names>E</given-names>
</name>
<name>
<surname>Peraita-Adrados</surname>
<given-names>R</given-names>
</name>
<name>
<surname>Sonka</surname>
<given-names>K</given-names>
</name>
<etal/>
</person-group>
<article-title>Kleine-Levin syndrome: an autoimmune hypothesis based on clinical and genetic analyses</article-title>
<source>Neurology</source>
<year>2002</year>
<month>Dec</month>
<volume>59</volume>
<issue>11</issue>
<fpage>1739</fpage>
<lpage>1745</lpage>
<pub-id pub-id-type="doi">10.1212/01.WNL.0000036605.89977.D0</pub-id>
<pub-id pub-id-type="pmid">12473762</pub-id>
</element-citation>
</ref>
<ref id="CIT0002">
<label>2</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Katz</surname>
<given-names>JD</given-names>
</name>
<name>
<surname>Ropper</surname>
<given-names>AH</given-names>
</name>
</person-group>
<article-title>Familial Kleine-Levin syndrome: two siblings with unusually long hypersomnic spells</article-title>
<source>Arch Neurol</source>
<year>2002</year>
<month>Dec</month>
<volume>59</volume>
<issue>12</issue>
<fpage>1959</fpage>
<lpage>1961</lpage>
<pub-id pub-id-type="doi">10.1001/archneur.59.12.1959</pub-id>
<pub-id pub-id-type="pmid">12470186</pub-id>
</element-citation>
</ref>
</ref-list>
</back>
</article>