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Fetal Acardia Syndrome in monozygotic twin pregnancy: Case report

Carvalho CM;
Freire SIS;
Maia MLP;
Freitas JMR;
Coelho LFO;
Júnior EP;
Pedrosa MS

Cristopher Mateus Carvalho

Sara Iasmim Santos Freire

Maria Luiza Peloso Maia

João Manoel Rodrigues de Freitas

Luiz Fernando de Oliveira Coelho

Eduardo Paulino Júnior

Moisés Salgado Pedrosa


Resumen

Fetal acardia is a rare complication that affects monochorionic/diaminiotic twin pregnancies and is characterized by the presence of a fetus with no heart (acardiac fetus) or a rudimentary heart (hemicardiac fetus). The objective of the present article is to present a case of fetal acardia with diagnosis confirmed by anatomopathological examination in which the "pump fetus" survived the pregnancy without specific treatment and without intercurrences.

 

DOI:https://doi.org/10.56238/interdiinovationscrese-057


Creative Commons License

Esta obra está bajo una licencia internacional Creative Commons Atribución-NoComercial 4.0.

Derechos de autor 2023 Cristopher Mateus Carvalho, Sara Iasmim Santos Freire, Maria Luiza Peloso Maia , João Manoel Rodrigues de Freitas, Luiz Fernando de Oliveira Coelho, Eduardo Paulino Júnior, Moisés Salgado Pedrosa

##plugins.themes.gdThemes.article.Authors##

  • Cristopher Mateus Carvalho
  • Sara Iasmim Santos Freire
  • Maria Luiza Peloso Maia
  • João Manoel Rodrigues de Freitas
  • Luiz Fernando de Oliveira Coelho
  • Eduardo Paulino Júnior
  • Moisés Salgado Pedrosa