Tratamiento quirúrgico de disección de aorta torácica ascendente en Sindrome de Marfán.

Authors

  • Efraín Montesinos Mosqueira
  • Julio C Vasquez Kobashigawa
  • Luis Rojas Peña
  • Julio Peralta Rodriguez

DOI:

https://doi.org/10.20453/rmh.v18i2.939

Abstract

Se presentan 5 casos consecutivos de pacientes con Síndrome de Marfan y disección de aorta torácica ascendente, quienes fueron tratados quirúrgicamente con reemplazo de raíz aórtica (operación modificada de Bentall). Todos los pacientes tuvieron plena recuperación y al seguimiento post alta realizan actividades de la vida diaria sin problemas.

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Published

2012-12-05

How to Cite

1.
Montesinos Mosqueira E, Vasquez Kobashigawa JC, Rojas Peña L, Peralta Rodriguez J. Tratamiento quirúrgico de disección de aorta torácica ascendente en Sindrome de Marfán. Rev Méd Hered [Internet]. 2012 Dec. 5 [cited 2025 Feb. 4];18(2):110. Available from: http://44.198.254.164/index.php/RMH/article/view/939

Issue

Vol. 18 No. 2 (2007): April - June

Section

BRIEF COMUNICATION

License

Authors assign their rights to the RMH so that may disseminate the article through the means at their disposal. The journal will provide forms of affidavit of authorship and authorization for the publication of the article, which shall be submitted with the manuscript. Authors retain the right to share, copy, distribute, perform and publicly communicate their article, or part of it, mentioning the original publication in the journal. 

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