<?xml version="1.0" encoding="ISO-8859-1"?><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">
<front>
<journal-meta>
<journal-id>2604-1227</journal-id>
<journal-title><![CDATA[Revista mexicana de oftalmología]]></journal-title>
<abbrev-journal-title><![CDATA[Rev. mex. oftalmol]]></abbrev-journal-title>
<issn>2604-1227</issn>
<publisher>
<publisher-name><![CDATA[Sociedad Mexicana de Oftalmología A.C.]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S2604-12272021000400167</article-id>
<article-id pub-id-type="doi">10.24875/rmo.m20000142</article-id>
<title-group>
<article-title xml:lang="es"><![CDATA[Síndrome de Aicardi: reporte de caso. Más allá de la oftalmología]]></article-title>
<article-title xml:lang="en"><![CDATA[Aicardi syndrome: a case report. Beyond ophthalmology]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Kim]]></surname>
<given-names><![CDATA[Hae Jin]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Lozano-Garza]]></surname>
<given-names><![CDATA[Rodrigo I.]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Dios-Cuadras]]></surname>
<given-names><![CDATA[Ulises de]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Guerrero-Becerril]]></surname>
<given-names><![CDATA[Jesús]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Urióstegui-Rojas]]></surname>
<given-names><![CDATA[Andrés]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Chacón-Camacho]]></surname>
<given-names><![CDATA[Oscar F.]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Graue-Wiechers]]></surname>
<given-names><![CDATA[Federico]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Hofmann-Blancas]]></surname>
<given-names><![CDATA[María E.]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Zenteno-Ruiz]]></surname>
<given-names><![CDATA[Juan C.]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
</contrib-group>
<aff id="Af1">
<institution><![CDATA[,Instituto de Oftalmología Fundación Conde de Valenciana Departamento de Retina y Vítreo ]]></institution>
<addr-line><![CDATA[Ciudad de México ]]></addr-line>
<country>México</country>
</aff>
<aff id="Af2">
<institution><![CDATA[,Instituto de Oftalmología Fundación Conde de Valenciana Departamento de Glaucoma ]]></institution>
<addr-line><![CDATA[Ciudad de México ]]></addr-line>
<country>México</country>
</aff>
<aff id="Af4">
<institution><![CDATA[,Instituto de Oftalmología Fundación Conde de Valenciana Departamento de Oftalmología Integral ]]></institution>
<addr-line><![CDATA[Ciudad de México ]]></addr-line>
<country>México</country>
</aff>
<aff id="Af5">
<institution><![CDATA[,Instituto de Oftalmología Fundación Conde de Valenciana Departamento de Genética ]]></institution>
<addr-line><![CDATA[Ciudad de México ]]></addr-line>
<country>México</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>08</month>
<year>2021</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>08</month>
<year>2021</year>
</pub-date>
<volume>95</volume>
<numero>4</numero>
<fpage>167</fpage>
<lpage>170</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_arttext&amp;pid=S2604-12272021000400167&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_abstract&amp;pid=S2604-12272021000400167&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_pdf&amp;pid=S2604-12272021000400167&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="es"><p><![CDATA[Resumen  Objetivo: El síndrome de Aicardi fue descrito en 1965 como una tríada de anormalidades que incluye agenesia parcial o total del cuerpo calloso, lagunas coriorretinianas y espasmos infantiles. Se presenta el caso de una paciente con diagnóstico de síndrome de Aicardi que debutó con manifestaciones neurológicas, por lo que se decidió su abordaje multidisciplinario.  Caso clínico: Paciente de sexo femenino, de 1 mes de edad, que llega al departamento de genética con antecedentes de epilepsia (espasmos infantiles), agenesia total de cuerpo calloso y disgenesia vertebral con escoliosis encontradas durante la evaluación neurológica previa. El examen oftalmológico reveló microftalmia en el ojo derecho, microcórnea en el ojo izquierdo presentó y resto del segmento anterior sin alteraciones. En la fundoscopia se observaron lesiones coriorretinianas compatibles con lagunas coriorretinianas, así como coloboma de nervio óptico, por lo que se diagnostica síndrome de Aicardi.  Conclusiones: Enfatizamos la importancia del examen oftalmológico completo en todos los pacientes para detectar de manera oportuna cualquier anormalidad, además de realizar siempre un abordaje sistémico que permita un diagnóstico sindromático, e individualizar el plan terapéutico.]]></p></abstract>
<abstract abstract-type="short" xml:lang="en"><p><![CDATA[Abstract  Purpose: Aicardi syndrome was originally described in 1965, as a triad of abnormalities that includes partial or total agenesis of the corpus callosum, chorioretinal lacunae, and infantile spasms.  Case report: A 1-month-old female was evaluated in the Genetics department with a history of epilepsy, total agenesis of the corpus callosum, and vertebral dysgenesis with scoliosis identified during a previous neurological evaluation. An ophthalmological examination revealed microphthalmia of the right eye and microcornea in the left eye; the rest of the anterior segment showed no alterations. Fundoscopy revealed chorioretinal lesions compatible with chorioretinal lacunae that integrated the diagnosis of Aicardi syndrome.  Conclusions: We emphasize the importance of a careful ophthalmologic examination in all patients to identify ophthalmological and systemic abnormalities at an early age and the development and implementation of an individualized therapy plan.]]></p></abstract>
<kwd-group>
<kwd lng="es"><![CDATA[Agenesia del cuerpo calloso]]></kwd>
<kwd lng="es"><![CDATA[Lagunas coriorretinianas]]></kwd>
<kwd lng="es"><![CDATA[Síndrome de Aicardi]]></kwd>
<kwd lng="en"><![CDATA[Agenesis of the corpus callosum]]></kwd>
<kwd lng="en"><![CDATA[Chorioretinal lacunae]]></kwd>
<kwd lng="en"><![CDATA[Aicardi syndrome]]></kwd>
</kwd-group>
</article-meta>
</front><back>
<ref-list>
<ref id="B1">
<label>1</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Aicardi]]></surname>
<given-names><![CDATA[J]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Aicardi syndrome]]></article-title>
<source><![CDATA[Brain Dev]]></source>
<year>2005</year>
<volume>27</volume>
<page-range>164-71</page-range></nlm-citation>
</ref>
<ref id="B2">
<label>2</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Fernández-Ramos]]></surname>
<given-names><![CDATA[JA]]></given-names>
</name>
<name>
<surname><![CDATA[López-Laso]]></surname>
<given-names><![CDATA[E]]></given-names>
</name>
<name>
<surname><![CDATA[Simón-De Las Heras]]></surname>
<given-names><![CDATA[R]]></given-names>
</name>
<name>
<surname><![CDATA[Camino-León]]></surname>
<given-names><![CDATA[R]]></given-names>
</name>
<name>
<surname><![CDATA[Guerra-García]]></surname>
<given-names><![CDATA[P]]></given-names>
</name>
<name>
<surname><![CDATA[Camacho-Salas]]></surname>
<given-names><![CDATA[A]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Aicardi syndrome:retrospective study of a series of seven case reports]]></article-title>
<source><![CDATA[Rev Neurol]]></source>
<year>2013</year>
<volume>57</volume>
<page-range>481-8</page-range></nlm-citation>
</ref>
<ref id="B3">
<label>3</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Sutton]]></surname>
<given-names><![CDATA[VR]]></given-names>
</name>
<name>
<surname><![CDATA[Hopkins]]></surname>
<given-names><![CDATA[BJ]]></given-names>
</name>
<name>
<surname><![CDATA[Eble]]></surname>
<given-names><![CDATA[TN]]></given-names>
</name>
<name>
<surname><![CDATA[Gambhir]]></surname>
<given-names><![CDATA[N]]></given-names>
</name>
<name>
<surname><![CDATA[Lewis]]></surname>
<given-names><![CDATA[RA]]></given-names>
</name>
<name>
<surname><![CDATA[Van den Veyver]]></surname>
<given-names><![CDATA[IB]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Facial and physical features of Aicardi syndrome:infants to teenagers]]></article-title>
<source><![CDATA[Am J Med Genet A]]></source>
<year>2005</year>
<volume>138A</volume>
<page-range>254-8</page-range></nlm-citation>
</ref>
<ref id="B4">
<label>4</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Kroner]]></surname>
<given-names><![CDATA[BL]]></given-names>
</name>
<name>
<surname><![CDATA[Preiss]]></surname>
<given-names><![CDATA[LR]]></given-names>
</name>
<name>
<surname><![CDATA[Ardini]]></surname>
<given-names><![CDATA[MA]]></given-names>
</name>
<name>
<surname><![CDATA[Gaillard]]></surname>
<given-names><![CDATA[WD]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[New incidence, prevalence, and survival of Aicardi syndrome from 408 cases]]></article-title>
<source><![CDATA[J Child Neurol]]></source>
<year>2008</year>
<volume>23</volume>
<page-range>531-5</page-range></nlm-citation>
</ref>
<ref id="B5">
<label>5</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Fruhman]]></surname>
<given-names><![CDATA[G]]></given-names>
</name>
<name>
<surname><![CDATA[Eble]]></surname>
<given-names><![CDATA[TN]]></given-names>
</name>
<name>
<surname><![CDATA[Gambhir]]></surname>
<given-names><![CDATA[N]]></given-names>
</name>
<name>
<surname><![CDATA[Sutton]]></surname>
<given-names><![CDATA[VR]]></given-names>
</name>
<name>
<surname><![CDATA[Van den Veyver]]></surname>
<given-names><![CDATA[IB]]></given-names>
</name>
<name>
<surname><![CDATA[Lewis]]></surname>
<given-names><![CDATA[RA]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Ophthalmologic findings in Aicardi syndrome]]></article-title>
<source><![CDATA[J AAPOS]]></source>
<year>2012</year>
<volume>16</volume>
<page-range>238-41</page-range></nlm-citation>
</ref>
<ref id="B6">
<label>6</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Cabrera]]></surname>
<given-names><![CDATA[MT]]></given-names>
</name>
<name>
<surname><![CDATA[Winn]]></surname>
<given-names><![CDATA[BJ]]></given-names>
</name>
<name>
<surname><![CDATA[Porco]]></surname>
<given-names><![CDATA[T]]></given-names>
</name>
<name>
<surname><![CDATA[Strominger]]></surname>
<given-names><![CDATA[Z]]></given-names>
</name>
<name>
<surname><![CDATA[Barkovich]]></surname>
<given-names><![CDATA[AJ]]></given-names>
</name>
<name>
<surname><![CDATA[Hoyt]]></surname>
<given-names><![CDATA[CS]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Laterality of brain and ocular lesions in Aicardi syndrome]]></article-title>
<source><![CDATA[Pediatr Neurol]]></source>
<year>2011</year>
<volume>45</volume>
<page-range>149-54</page-range></nlm-citation>
</ref>
<ref id="B7">
<label>7</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Shah]]></surname>
<given-names><![CDATA[PK]]></given-names>
</name>
<name>
<surname><![CDATA[Narendran]]></surname>
<given-names><![CDATA[V]]></given-names>
</name>
<name>
<surname><![CDATA[Kalpana]]></surname>
<given-names><![CDATA[N]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Aicardi syndrome:the importance of an ophthalmologist in its diagnosis]]></article-title>
<source><![CDATA[Indian J Ophthalmol]]></source>
<year>2009</year>
<volume>57</volume>
<page-range>234</page-range></nlm-citation>
</ref>
<ref id="B8">
<label>8</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Martel]]></surname>
<given-names><![CDATA[JN]]></given-names>
</name>
<name>
<surname><![CDATA[Rutar]]></surname>
<given-names><![CDATA[T]]></given-names>
</name>
<name>
<surname><![CDATA[Lujan]]></surname>
<given-names><![CDATA[BJ]]></given-names>
</name>
<name>
<surname><![CDATA[de Alba Campomanes]]></surname>
<given-names><![CDATA[A]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[(2011). Chorioretinal architecture in Aicardi syndrome:an optical coherence tomography and fluorescein angiography study]]></article-title>
<source><![CDATA[J AAPOS]]></source>
<year>2011</year>
<volume>15</volume>
<page-range>308-10</page-range></nlm-citation>
</ref>
<ref id="B9">
<label>9</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Galdós]]></surname>
<given-names><![CDATA[M]]></given-names>
</name>
<name>
<surname><![CDATA[Martínez]]></surname>
<given-names><![CDATA[R]]></given-names>
</name>
<name>
<surname><![CDATA[Prats]]></surname>
<given-names><![CDATA[JM]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Clinical outcome of distinct Aicardi syndrome phenotypes]]></article-title>
<source><![CDATA[Arch Soc Esp Oftalmol]]></source>
<year>2008</year>
<volume>83</volume>
<page-range>29-36</page-range></nlm-citation>
</ref>
<ref id="B10">
<label>10</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Lund]]></surname>
<given-names><![CDATA[C]]></given-names>
</name>
<name>
<surname><![CDATA[Striano]]></surname>
<given-names><![CDATA[P]]></given-names>
</name>
<name>
<surname><![CDATA[Sorte]]></surname>
<given-names><![CDATA[HS]]></given-names>
</name>
<name>
<surname><![CDATA[Parisi]]></surname>
<given-names><![CDATA[P]]></given-names>
</name>
<name>
<surname><![CDATA[Iacomino]]></surname>
<given-names><![CDATA[M]]></given-names>
</name>
<name>
<surname><![CDATA[Sheng]]></surname>
<given-names><![CDATA[Y]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Exome sequencing fails to identify the genetic cause of Aicardi syndrome]]></article-title>
<source><![CDATA[Mol Syndromol]]></source>
<year>2016</year>
<volume>7</volume>
<page-range>234-8</page-range></nlm-citation>
</ref>
</ref-list>
</back>
</article>
