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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-b</article-id>
<article-id pub-id-type="doi">10.15844/pedneurbriefs-10-9-10</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>Hypothyroidism and Chromosome 21 Deletion</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>71</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="10.1002/(SICI)1096-8628(19960823)64:3&#x003C;501::AID-AJMG11&#x003E;3.0.CO;2-P" vol="64" page="501">
<article-title>Deletion of chromosome 21 in a girl with congenital hypothyroidism and mild mental retardation</article-title>
</related-article>
<abstract abstract-type="web-summary" specific-use="electronic-only">
<p>A 12-year-old mentally retarded girl with a large deletion of the long arm of chromosome 21 and congenital hypothyroidism is reported from the Department of Clinical Genetics and Pediatrics, University Hospital, Uppsala, Sweden.</p>
</abstract>
<kwd-group>
<kwd>Congenital Hypothyroidism</kwd>
<kwd>Down Syndrome</kwd>
<kwd>Chromosome 21</kwd>
</kwd-group>
</article-meta>
</front>
<body>
<p>A 12-year-old mentally retarded girl with a large deletion of the long arm of chromosome 21 and congenital hypothyroidism is reported from the Department of Clinical Genetics and Pediatrics, University Hospital, Uppsala, Sweden. Despite the large chromosome deletion, the degree of mental retardation was mild and severe manifestations of Down syndrome were absent. The proximal part of the long arm of chromosome 21 does not include the genes responsible for severe clinical effects seen in Down syndrome. Congenital hypothyroidism in this patient might indicate the importance of genes on chromosome 21 for thyroid function. [<xref ref-type="bibr" rid="CIT0001">1</xref>]</p>
<p>COMMENT. Patients with Down syndrome often suffer from thyroid disorders and congenital hypothyroidism is much more common in DS than in normal individuals. It is likely that the congenital hypothyroidism in the above patient was related to the chromosome 21 abnormality.</p>
<p>The clinical manifestations of partial deletion of chromosome 21 have included mild mental retardation, short stature, obesity, hypotonia, prominent forehead, downslanting palpebral fissures, hyperopia, large/low set ears, high arched palate, prognathism, long/slender hands, short 5th finger, broad feet, large stiff joints, and congenital hypothyroidism.</p>
</body>
<back>
<ref-list>
<ref id="CIT0001">
<label>1</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Ahlbom</surname>
<given-names>BE</given-names>
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<article-title>Deletion of chromosome 21 in a girl with congenital hypothyroidism and mild mental retardation</article-title>
<source>Am J Med Genet</source>
<year>1996</year>
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<day>23</day>
<volume>64</volume>
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<pub-id pub-id-type="pmid">8862630</pub-id>
<pub-id pub-id-type="doi">10.1002/(SICI)1096-8628(19960823)64:3&#x003C;501::AID-AJMG11&#x003E;3.0.CO;2-P</pub-id>
</element-citation>
</ref>
</ref-list>
</back>
</article>
