Fetal Acardia Syndrome in monozygotic twin pregnancy: Case report

Autores/as

  • 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

Palabras clave:

Diamniotic, Twin pregnancy, Monochorionic, Fetal Acardia Syndrome

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

Publicado

2023-11-08

Cómo citar

Fetal Acardia Syndrome in monozygotic twin pregnancy: Case report. (2023). Seven Editora. https://sevenpublicacoes.com.br/editora/article/view/2949