<?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>1699-695X</journal-id>
<journal-title><![CDATA[Revista Clínica de Medicina de Familia]]></journal-title>
<abbrev-journal-title><![CDATA[Rev Clin Med Fam]]></abbrev-journal-title>
<issn>1699-695X</issn>
<publisher>
<publisher-name><![CDATA[Sociedad Española de Medicina de Familia y Comunitaria]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S1699-695X2021000200011</article-id>
<title-group>
<article-title xml:lang="es"><![CDATA[Síndrome de Zinner: monorrenos especiales]]></article-title>
<article-title xml:lang="en"><![CDATA[Zinner syndrome: special single kidney patients]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Córdoba-Quishpe]]></surname>
<given-names><![CDATA[Golda Alexandra]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Sierra-Santos]]></surname>
<given-names><![CDATA[Lucía]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
<xref ref-type="aff" rid="Aaf"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Maqueda-Zamora]]></surname>
<given-names><![CDATA[Gloria]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[García-Morales]]></surname>
<given-names><![CDATA[Antonio]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
</contrib-group>
<aff id="Af1">
<institution><![CDATA[,Hospital Universitario Ramón y Cajal Centro de Salud Mar Báltico ]]></institution>
<addr-line><![CDATA[Madrid ]]></addr-line>
<country>España</country>
</aff>
<aff id="Af2">
<institution><![CDATA[,Consultorio El Boalo  ]]></institution>
<addr-line><![CDATA[Madrid ]]></addr-line>
<country>España</country>
</aff>
<aff id="Af3">
<institution><![CDATA[,Sociedad Española de Medicina Familiar y Comunitaria Grupo de Trabajo de Genética Clínica y Cáncer Hereditario ]]></institution>
<addr-line><![CDATA[ ]]></addr-line>
</aff>
<aff id="Af4">
<institution><![CDATA[,Hospital Universitario La Paz Consultorio El Boalo ]]></institution>
<addr-line><![CDATA[Madrid ]]></addr-line>
<country>España</country>
</aff>
<aff id="Af5">
<institution><![CDATA[,Hospital Universitario Ramón y Cajal Centro de Salud Barajas ]]></institution>
<addr-line><![CDATA[Madrid ]]></addr-line>
<country>España</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>00</month>
<year>2021</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>00</month>
<year>2021</year>
</pub-date>
<volume>14</volume>
<numero>2</numero>
<fpage>100</fpage>
<lpage>102</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://scielo.isciii.es/scielo.php?script=sci_arttext&amp;pid=S1699-695X2021000200011&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://scielo.isciii.es/scielo.php?script=sci_abstract&amp;pid=S1699-695X2021000200011&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://scielo.isciii.es/scielo.php?script=sci_pdf&amp;pid=S1699-695X2021000200011&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="es"><p><![CDATA[RESUMEN El síndrome de Zinner es una rara entidad urológica caracterizada por la dilatación quística unilateral de una vesícula seminal junto con atrofia o agenesia renal ipsilateral. Los pacientes permanecen asintomáticos en la mayoría de los casos y su diagnóstico es incidental. El tratamiento de elección es quirúrgico cuando presentan sintomatología o se ve afectada la fertilidad del paciente. Presentamos el caso de un paciente de 13 años, monorreno de nacimiento, asintomático, sin otros antecedentes personales de interés, al que, durante un examen rutinario de su patología de base, se le realiza ecografía abdominal en la que se visualiza un probable quiste ureteral con una dilatación de la vesícula seminal compatible con un probable síndrome de Zinner.]]></p></abstract>
<abstract abstract-type="short" xml:lang="en"><p><![CDATA[ABSTRACT Zinner syndrome is a rare urological entity characterized by unilateral cystic dilation of a seminal vesicle together with atrophy or ipsilateral renal agenesis. Patients remain asymptomatic in most cases and their diagnosis is incidental. The treatment of choice is surgical when symptoms occur or affect the patient´s fertility. We report the case of a 13-year-old asymptomatic boy born with a single-kidney with no other personal history of interest. During a routine examination of his underlying pathology, abdominal ultrasound was performed where a probable ureteral cyst with seminal vesicle dilation compatible with probable Zinner syndrome was observed.]]></p></abstract>
<kwd-group>
<kwd lng="es"><![CDATA[vesículas seminales]]></kwd>
<kwd lng="es"><![CDATA[agenesia renal unilateral]]></kwd>
<kwd lng="es"><![CDATA[anomalías congénitas]]></kwd>
<kwd lng="en"><![CDATA[Congenital Abnormalities]]></kwd>
<kwd lng="en"><![CDATA[Seminal Vesicles]]></kwd>
<kwd lng="en"><![CDATA[Unilateral Renal Agenesis]]></kwd>
</kwd-group>
</article-meta>
</front><back>
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