Síndrome da Acardia Fetal em gestação gemelar monozigótica: relato de caso

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

DOI:

https://doi.org/10.54022/shsv4n1-011

Keywords:

diamniótica, gestação gemelar, monocoriônica, Síndrome da Acardia Fetal

Abstract

A acardia fetal é uma complicação rara que afeta gestações gemelares monocoriônicas/diaminióticas e caracteriza-se pela presença de um feto que não apresenta coração (feto acárdico) ou apresenta um coração rudimentar (feto hemicárdico). O objetivo do presente artigo é apresentar um caso de acardia fetal com diagnóstico firmado por exame anatomopatológico no qual o “feto bomba” sobreviveu à gestação sem tratamento específico e sem intercorrências.

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Published

2023-03-02

How to Cite

Carvalho, C. M., Freire, S. I. S., Maia, M. L. P., de Freitas, J. M. R., Coelho, L. F. de O., Paulino Júnior, E., & Pedrosa, M. S. (2023). Síndrome da Acardia Fetal em gestação gemelar monozigótica: relato de caso . STUDIES IN HEALTH SCIENCES, 4(1), 104–115. https://doi.org/10.54022/shsv4n1-011