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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-2-53-a</article-id>
<article-id pub-id-type="doi">10.15844/pedneurbriefs-2-7-7</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Developmental 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>Hypomelanosis of Ito</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>07</month>
<year>1988</year>
</pub-date>
<pub-date date-type="pub" publication-format="electronic">
<day>01</day>
<month>08</month>
<year>2016</year>
</pub-date>
<volume>2</volume>
<issue>7</issue>
<fpage>53</fpage>
<lpage>53</lpage>
<permissions>
<copyright-statement>Copyright: &#x00A9; 1988 The Author(s)</copyright-statement>
<copyright-year>1988</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="pmid" xlink:href="3383022" vol="15" page="124">
<article-title>Hypomelanosis of Ito. Neurological complications in 34 cases</article-title>
</related-article>
<abstract abstract-type="web-summary" specific-use="electronic-only">
<p>The neurological complications in 34 Spanish children with hypomelanosis of Ito are described from the Paediatric Neurology Service, Hospital Infantil La Paz, and La Universidad Autonoma, Madrid, Spain.</p>
</abstract>
<kwd-group>
<kwd>Hypomelanosis</kwd>
<kwd>Angiomatous Nevi</kwd>
<kwd>Fair-Skinned Individuals</kwd>
</kwd-group>
</article-meta>
</front>
<body>
<p>The neurological complications in 34 Spanish children with hypomelanosis of Ito are described from the Paediatric Neurology Service, Hospital Infantil La Paz, and La Universidad Autonoma, Madrid, Spain. Most were referred because of mental retardation (65%) and seizures (53%), and the ages at time of the first visit were 2 months to 10 years. Skin lesions, observed within the first year of life in 70% of patients, consisted of hypomelanotic depigmented patches, cafe-au-lait spots, and angiomatous nevi; changes in hair color and alopecia also occurred. Noncutaneous abnormalities, observed in 94%, included macrocephaly, microcephaly, hemihypertrophy, kyphoscoliosis, coarse facial features, and hypertelorism. Autosomal dominant inheritance was demonstrated in some. [<xref ref-type="bibr" rid="CIT0001">1</xref>]</p>
<disp-quote>
<p>
<bold>COMMENT</bold>. The incidence of this disease was estimated at 1 per 1000 new patients consulting a pediatric neurology service, or 1 per 10,000 unselected patients in a children&#x0027;s hospital. It affects all races, but fair-skinned individuals may require a Woods lamp examination to detect the cutaneous lesions.</p>
</disp-quote>
</body>
<back>
<ref-list>
<ref id="CIT0001">
<label>1</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Pascual-Castroviejo</surname>
<given-names>I</given-names>
</name>
<name>
<surname>L&#x00F3;pez-Rodriguez</surname>
<given-names>L</given-names>
</name>
<name>
<surname>de la Cruz Medina</surname>
<given-names>M</given-names>
</name>
<name>
<surname>Salamanca-Maesso</surname>
<given-names>C</given-names>
</name>
<name>
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<given-names>C</given-names>
</name>
</person-group>
<article-title>Hypomelanosis of Ito. Neurological complications in 34 cases</article-title>
<source>Can J Neurol Sci</source>
<year>1988</year>
<month>May</month>
<volume>15</volume>
<issue>2</issue>
<fpage>124</fpage>
<lpage>9</lpage>
<pub-id pub-id-type="pmid">3383022</pub-id>
</element-citation>
</ref>
</ref-list>
</back>
</article>
