<?xml version="1.0" encoding="UTF-8"?>
<!DOCTYPE article PUBLIC "-//NLM//DTD JATS (Z39.96) Journal Publishing DTD v1.0 20120330//EN" "http://jats.nlm.nih.gov/publishing/1.0/JATS-journalpublishing1.dtd">
<article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" article-type="article-commentary" dtd-version="1.0" xml:lang="en">
<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="ppub">1043-3155</issn>
<issn pub-type="epub">2166-6482</issn>
<issn-l>1043-3155</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-29-83</article-id>
<article-id pub-id-type="doi">10.15844/pedneurbriefs-29-11-2</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Neuromuscular 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>Hereditary Neuropathy with Liability to Pressure Palsies</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author" corresp="yes">
<name>
<surname>Choi</surname>
<given-names>Hyoung Won</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 contrib-type="author">
<name>
<surname>Kuntz</surname>
<given-names>Nancy L.</given-names>
</name>
<degrees>MD</degrees>
<xref ref-type="aff" rid="AF0001">1</xref>
<xref ref-type="aff" rid="AF0002">2</xref>
</contrib>
</contrib-group>
<aff id="AF0001">
<label>1</label>Division of Neurology, Ann &#x0026; Robert H. Lurie Children&#x0027;s Hospital of Chicago, 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. Hyoung Won Choi, E-mail: <email xlink:href="chyoungwon@luriechildrens.org">chyoungwon@luriechildrens.org</email>
</corresp>
</author-notes>
<pub-date date-type="pub" publication-format="print">
<month>11</month>
<year>2015</year>
</pub-date>
<pub-date date-type="pub" publication-format="electronic">
<day>17</day>
<month>12</month>
<year>2015</year>
</pub-date>
<volume>29</volume>
<issue>11</issue>
<fpage>83</fpage>
<lpage>83</lpage>
<history>
<date date-type="received">
<day>01</day>
<month>12</month>
<year>2015</year>
</date>
<date date-type="accepted">
<day>10</day>
<month>12</month>
<year>2015</year>
</date>
</history>
<permissions>
<copyright-statement>Copyright: &#x00A9; 2015 The Author(s)</copyright-statement>
<copyright-year>2015</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="10.1016/0092-8674(93)90058-X" vol="72" page="143">
<article-title>DNA deletion associated with hereditary neuropathy with liability to pressure palsies</article-title>
</related-article>
<abstract abstract-type="web-summary" specific-use="electronic-only">
<p>Investigators from 4 pediatric hospitals in Canada analyzed the clinical presentation and electrophysiological data of 12 children with hereditary neuropathy with liability to pressure palsies (HNPP), caused by PMP22 gene deletion.</p>
</abstract>
<kwd-group>
<kwd>Mononeuropathies</kwd>
<kwd>HNPP</kwd>
<kwd>Childhood</kwd>
<kwd>PMP22 Protein</kwd>
</kwd-group>
</article-meta>
</front>
<body>
<p>Investigators from 4 pediatric hospitals in Canada analyzed the clinical presentation and electrophysiological data of 12 children with hereditary neuropathy with liability to pressure palsies (HNPP), caused by PMP22 gene deletion. Peroneal palsy was the most common presentation (42%) followed by brachial plexus palsy in 25% of their cases. Complete nerve conduction studies were available in 10/12 cases and it demonstrated 3 major patterns: multifocal demyelination at areas of nerve entrapment without generalized demyelinating polyneuropathy (20%), isolated generalized sensorimotor polyneuropathy (20%), combined focal demyelination at the area of entrapment and demyelinating polyneuropathy (60%). All patients had electrophysiological evidence of unilateral or bilateral carpal tunnel syndrome, although it was not always symptomatic. Electrophysiological findings are useful in diagnosis of HNPP, especially in children with heterogeneous clinical presentation. [<xref ref-type="bibr" rid="CIT0001">1</xref>]</p>
<p>COMMENTARY. HNPP is the third most common type of hereditary motor and sensory neuropathy [<xref ref-type="bibr" rid="CIT0001">1</xref>]. The typical clinical presentation is usually reported as a recurrent, painless monoparesis, with its first attack being in second or third decades [<xref ref-type="bibr" rid="CIT0002">2</xref>]. The diagnosis is usually made in early adulthood unless there is a family history. A smaller case series published by Potulska-Chromik et al. about 7 children with genetically confirmed HNPP provides similar observations [<xref ref-type="bibr" rid="CIT0003">3</xref>]. Their clinical presentation varied from mononeuropathy to brachial plexopathy, with recurrent episodes in 4 out of 7 patients. An earlier study that included 48 children with HNPP documented &#x003E; 50% of children with HNPP has delayed onset of walking (after 15 months of age) [<xref ref-type="bibr" rid="CIT0004">4</xref>]. Based on the results of the study, the authors advocate testing PMP22 gene deletion for any children with unexplained mononeuropathy or multifocal neuropathy to facilitate appropriate care and genetic counseling for these patients. The paper alerts child neurologists to consider the possibility of HNPP even in young children with a negative family history when they present with the typical compressive nerve palsy.</p>
</body>
<back>
<sec>
<title>Disclosures</title>
<p>The author(s) have declared that no competing interests exist.</p>
</sec>
<ref-list>
<ref id="CIT0001">
<label>1</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Chance</surname>
<given-names>PF</given-names>
</name>
<name>
<surname>Alderson</surname>
<given-names>MK</given-names>
</name>
<name>
<surname>Leppig</surname>
<given-names>KA</given-names>
</name>
<name>
<surname>Lensch</surname>
<given-names>MW</given-names>
</name>
<name>
<surname>Matsunami</surname>
<given-names>N</given-names>
</name>
<name>
<surname>Smith</surname>
<given-names>B</given-names>
</name>
<etal/>
</person-group>
<article-title>DNA deletion associated with hereditary neuropathy with liability to pressure palsies</article-title>
<source>Cell</source>
<year>1993</year>
<month>Jan</month>
<volume>72</volume>
<issue>1</issue>
<fpage>143</fpage>
<lpage>151</lpage>
<pub-id pub-id-type="doi">10.1016/0092-8674(93)90058-X</pub-id>
<pub-id pub-id-type="pmid">8422677</pub-id>
</element-citation>
</ref>
<ref id="CIT0002">
<label>2</label>
<element-citation publication-type="book">
<person-group person-group-type="editor">
<name>
<surname>Pagon</surname>
<given-names>RA</given-names>
</name>
<name>
<surname>Adam</surname>
<given-names>MP</given-names>
</name>
<name>
<surname>Ardinger</surname>
<given-names>HH</given-names>
</name>
<name>
<surname>Wallace</surname>
<given-names>SE</given-names>
</name>
<name>
<surname>Amemiya</surname>
<given-names>A</given-names>
</name>
<name>
<surname>Bean</surname>
<given-names>LJ</given-names>
</name>
<etal/>
</person-group>
<article-title>Hereditary Neuropathy with Liability to Pressure Palsies. GeneReviews(&#x00AE;) [Internet]</article-title>
<publisher-loc>Seattle (WA)</publisher-loc>
<publisher-name>University of Washington, Seattle</publisher-name>
<fpage>1993</fpage>
<lpage>2015</lpage>
</element-citation>
</ref>
<ref id="CIT0003">
<label>3</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Potulska-Chromik</surname>
<given-names>A</given-names>
</name>
<name>
<surname>Sinkiewicz-Darol</surname>
<given-names>E</given-names>
</name>
<name>
<surname>Ryniewicz</surname>
<given-names>B</given-names>
</name>
<name>
<surname>Lipowska</surname>
<given-names>M</given-names>
</name>
<name>
<surname>Kabzi&#324;ska</surname>
<given-names>D</given-names>
</name>
<name>
<surname>Kocha&#324;ski</surname>
<given-names>A</given-names>
</name>
<etal/>
</person-group>
<article-title>Clinical, electrophysiological, and molecular findings in early onset hereditary neuropathy with liability to pressure palsy</article-title>
<source>Muscle Nerve</source>
<year>2014</year>
<month>Dec</month>
<volume>50</volume>
<issue>6</issue>
<fpage>914</fpage>
<lpage>918</lpage>
<pub-id pub-id-type="doi">10.1002/mus.24250</pub-id>
<pub-id pub-id-type="pmid">24668782</pub-id>
</element-citation>
</ref>
<ref id="CIT0004">
<label>4</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Saporta</surname>
<given-names>AS</given-names>
</name>
<name>
<surname>Sottile</surname>
<given-names>SL</given-names>
</name>
<name>
<surname>Miller</surname>
<given-names>LJ</given-names>
</name>
<name>
<surname>Feely</surname>
<given-names>SM</given-names>
</name>
<name>
<surname>Siskind</surname>
<given-names>CE</given-names>
</name>
<name>
<surname>Shy</surname>
<given-names>ME</given-names>
</name>
</person-group>
<article-title>Charcot-Marie-Tooth disease subtypes and genetic testing strategies</article-title>
<source>Ann Neurol</source>
<year>2011</year>
<month>Jan</month>
<volume>69</volume>
<issue>1</issue>
<fpage>22</fpage>
<lpage>33</lpage>
<pub-id pub-id-type="doi">10.1002/ana.22166</pub-id>
<pub-id pub-id-type="pmid">21280073</pub-id>
</element-citation>
</ref>
</ref-list>
</back>
</article>
