<?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>2393-6797</journal-id>
<journal-title><![CDATA[Revista Uruguaya de Medicina Interna ]]></journal-title>
<abbrev-journal-title><![CDATA[Rev. Urug. Med. Int.]]></abbrev-journal-title>
<issn>2393-6797</issn>
<publisher>
<publisher-name><![CDATA[Sociedad de Medicina Interna del Uruguay]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S2393-67972021000200052</article-id>
<article-id pub-id-type="doi">10.26445/06.02.7</article-id>
<title-group>
<article-title xml:lang="es"><![CDATA[Abruptio placentae y trombofilia hereditaria]]></article-title>
<article-title xml:lang="en"><![CDATA[Abruptio placentae and hereditary thrombophilia]]></article-title>
<article-title xml:lang="pt"><![CDATA[Abruptio placentae e trombofilia hereditária]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Morán]]></surname>
<given-names><![CDATA[Rosario]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
</contrib-group>
<aff id="Af1">
<institution><![CDATA[,Universidad de la República Hospital de Clínicas Facultad de Medicina]]></institution>
<addr-line><![CDATA[ ]]></addr-line>
<country>Uruguay</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>07</month>
<year>2021</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>07</month>
<year>2021</year>
</pub-date>
<volume>6</volume>
<numero>2</numero>
<fpage>52</fpage>
<lpage>55</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.edu.uy/scielo.php?script=sci_arttext&amp;pid=S2393-67972021000200052&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.edu.uy/scielo.php?script=sci_abstract&amp;pid=S2393-67972021000200052&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.edu.uy/scielo.php?script=sci_pdf&amp;pid=S2393-67972021000200052&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="es"><p><![CDATA[Resumen: El abruptio placentae o desprendimiento prematuro de placenta normoinserta se define como el desprendimiento parcial o completo de la placenta normalmente implantada que ocurre antes del parto en embarazos mayores a 20 semanas. Entidad de elevada morbimortalidad (75%). La pato-fisiología es multifactorial, disminución de la invasión trofoblástica de las arterias espirales, disfunción endotelial y activación anormal de la coagulación a nivel de la interface materno-fetal. Es controversial si la trombofilia hereditaria contribuye a este proceso y de ser así como lo haría. Se realiza una revisión del tema con recomendaciones de estudio y tratamiento en pacientes que tienen esta patología.]]></p></abstract>
<abstract abstract-type="short" xml:lang="en"><p><![CDATA[Abstract: Abruptio placentae or premature detachment of the normoinserted placenta is defined as partial or complete detachment of the normally implanted placenta that occurs before delivery in pregnancies greater than 20 weeks. Entity with high morbidity and mortality (75%). The pathophysiology is multifactorial, decreased trophoblastic invasion of the spiral arteries, endothelial dysfunction and abnormal activation of coagulation at the level of the maternal-fetal interface. It is controversial whether and if hereditary thrombophilia contributes to this process. A review of the subject is carried out with study and treatment recommendations in patients who have this pathology.]]></p></abstract>
<abstract abstract-type="short" xml:lang="pt"><p><![CDATA[Resumo: O descolamento da placenta ou descolamento prematuro da placenta normoinserida é definido como o descolamento parcial ou completo da placenta normalmente implantada que ocorre antes do parto em gestações com mais de 20 semanas. Entidade com alta morbimortalidade (75%). A fisiopatologia é multifatorial, diminuição da invasão trofoblástica das artérias espirais, disfunção endotelial e ativação anormal da coagulação ao nível da interface materno-fetal. É controverso se e se a trombofilia hereditária contribui para esse processo. É feita uma revisão do assunto com recomendações de estudo e tratamento em pacientes portadores dessa patologia.]]></p></abstract>
<kwd-group>
<kwd lng="es"><![CDATA[abruptio placentae]]></kwd>
<kwd lng="es"><![CDATA[trombofilia hereditaria]]></kwd>
<kwd lng="en"><![CDATA[abruptio placentae]]></kwd>
<kwd lng="en"><![CDATA[hereditary thrombophilia]]></kwd>
<kwd lng="pt"><![CDATA[descolamento da placenta]]></kwd>
<kwd lng="pt"><![CDATA[trombofilia hereditária]]></kwd>
</kwd-group>
</article-meta>
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