<?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>1870-7203</journal-id>
<journal-title><![CDATA[Acta médica Grupo Ángeles]]></journal-title>
<abbrev-journal-title><![CDATA[Acta méd. Grupo Ángeles]]></abbrev-journal-title>
<issn>1870-7203</issn>
<publisher>
<publisher-name><![CDATA[Grupo Ángeles, Servicios de Salud]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S1870-72032022000400353</article-id>
<article-id pub-id-type="doi">10.35366/107122</article-id>
<title-group>
<article-title xml:lang="es"><![CDATA[Síndrome de Mayer-Rokitansky-Küster-Hauser]]></article-title>
<article-title xml:lang="en"><![CDATA[Mayer-Rokitansky-Küster-Hauser syndrome]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Mina Romero]]></surname>
<given-names><![CDATA[Elizabeth]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Álvarez Domínguez]]></surname>
<given-names><![CDATA[Sergio]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Valencia Arana]]></surname>
<given-names><![CDATA[Carlos Andrés]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Murúa Millán]]></surname>
<given-names><![CDATA[Oscar Abelardo]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Piña Ramírez]]></surname>
<given-names><![CDATA[Luis Eduardo]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Gómez Pérez]]></surname>
<given-names><![CDATA[María de Guadalupe]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
</contrib-group>
<aff id="Af1">
<institution><![CDATA[,Universidad La Salle Facultad Mexicana de Medicina ]]></institution>
<addr-line><![CDATA[Ciudad de México ]]></addr-line>
<country>Mexico</country>
</aff>
<aff id="Af2">
<institution><![CDATA[,Hospital Angeles Pedregal  ]]></institution>
<addr-line><![CDATA[Ciudad de México ]]></addr-line>
<country>México</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>12</month>
<year>2022</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>12</month>
<year>2022</year>
</pub-date>
<volume>20</volume>
<numero>4</numero>
<fpage>353</fpage>
<lpage>355</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_arttext&amp;pid=S1870-72032022000400353&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_abstract&amp;pid=S1870-72032022000400353&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_pdf&amp;pid=S1870-72032022000400353&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="es"><p><![CDATA[Resumen:  Introducción:  El síndrome de Mayer-Rokitansky-Ku&#776;ster-Hauser (también conocido como aplasia mu&#776;lleriana) es una rara anomalía congénita del tracto genital, de etiología desconocida, se caracteriza por la ausencia congénita del útero, cérvix y porción superior de la vagina.  Caso clínico:  Paciente femenino de 16 años de edad que presenta amenorrea primaria, perfil hormonal normal, desarrollo sexual adecuado Tanner 5, cariotipo 46 XX. Se realiza resonancia magnética, donde se detecta ausencia de útero y de los dos tercios proximales de la vagina.  Conclusión:  La resonancia magnética es una prueba diagnóstica que brinda gran detalle anatómico del útero y vagina, permitiendo caracterizar y clasificar correctamente a las anomalías mu&#776;llerianas.]]></p></abstract>
<abstract abstract-type="short" xml:lang="en"><p><![CDATA[Abstract:  Introduction:  Mayer-Rokitansky-Küster-Hauser syndrome (also known as müllerian aplasia) is a rare congenital anomaly of the tract genital, of unknown etiology, characterized by the congenital absence of the uterus, cervix and upper portion of the vagina.  Clinical case:  A 16-year-old female patient with primary amenorrhea, normal hormonal profile, adequate sexual development Tanner 5, 46 XX karyotype. A magnetic sound is performed where the absence of the uterus and the proximal two-thirds of the vagina are detected.  Conclusion:  Magnetic resonance is a diagnostic test that provides great anatomical detail of the uterus and vagina, allowing to correctly characterize and classify Müllerian anomalies.]]></p></abstract>
<kwd-group>
<kwd lng="es"><![CDATA[Síndrome de Rokitansky]]></kwd>
<kwd lng="es"><![CDATA[resonancia magnética]]></kwd>
<kwd lng="es"><![CDATA[malformaciones uterinas]]></kwd>
<kwd lng="es"><![CDATA[malformaciones mu&#776;llerianas]]></kwd>
<kwd lng="en"><![CDATA[Rokitansky syndrome]]></kwd>
<kwd lng="en"><![CDATA[magnetic resonance imaging]]></kwd>
<kwd lng="en"><![CDATA[uterine malformations]]></kwd>
<kwd lng="en"><![CDATA[mu&#776;llerian malformations]]></kwd>
</kwd-group>
</article-meta>
</front><back>
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</ref-list>
</back>
</article>
