2015
DOI: 10.1590/s1519-38292015000400008
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Manejo obstétrico de la deficiencia hereditaria de antitrombina durante el embarazo y puerperio. Dos casos clínicos

Abstract: Resumen Introducción: la deficiencia de antitrombina III hereditaria es una rara enfermedad que afecta al 0.02-0.2% de la población. Puede presentar mayor frecuencia de complicaciones y resultados adversos tanto en la madre como en el feto. Se presenta el manejo obstétrico de dos gestaciones consecutivas en una mujer con deficiencia de antitrombina III. Descripción: en ambos embarazos la madre realiza profilaxis de la enfermedad tromboembólica con heparina de bajo peso molecular para evitar la aparición de e… Show more

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“…Thrombosis is considered a multicausal pathology, and in recent years, more profound knowledge about its etiology has been obtained, as well as several factors that contribute to its incidence. Moreover, inheritance combined with genetic factors related to thrombophilia increases the risk of thrombotic episode occurrence [15] . In the early 19th century, Virchow described the mechanisms of thrombosis and reported a state of "altered blood composition", now called the hypercoagulable state.…”
Section: Pathology Mechanism and Complicationsmentioning
confidence: 99%
“…Thrombosis is considered a multicausal pathology, and in recent years, more profound knowledge about its etiology has been obtained, as well as several factors that contribute to its incidence. Moreover, inheritance combined with genetic factors related to thrombophilia increases the risk of thrombotic episode occurrence [15] . In the early 19th century, Virchow described the mechanisms of thrombosis and reported a state of "altered blood composition", now called the hypercoagulable state.…”
Section: Pathology Mechanism and Complicationsmentioning
confidence: 99%