Literature DB >> 19816031

Dichorionic triamniotic triplet pregnancy complicated by acardius acormus.

Khalil Abi-Nader1, Sara M Whitten, Elisa Filippi, Rosemary Scott, Eric Jauniaux.   

Abstract

This report describes an acardiac fetus of the acormus phenotype in a triplet pregnancy. The diagnosis was confirmed at 15 weeks. In the absence of signs of heart failure in the co-fetus the pregnancy was managed conservatively. The pregnancy was complicated by preterm labour and the fetuses were delivered at 26+5 weeks. The prenatal diagnosis of the acormus phenotype with a well-developed cephalic pole is extremely rare and has never been described antenatally in a higher order multiple pregnancy. We suggest that this rare acardiac fetus phenotype may have a different pathophysiology than those of other phenotypes. The report also summarizes the perinatal outcomes of triplet pregnancies complicated by an acardiac fetus, where the median gestational age at delivery is 26-27 weeks, and discusses the possible therapeutic interventions. 2009 S. Karger AG, Basel.

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Year:  2009        PMID: 19816031     DOI: 10.1159/000236360

Source DB:  PubMed          Journal:  Fetal Diagn Ther        ISSN: 1015-3837            Impact factor:   2.587


  2 in total

1.  Hypothesized pathogenesis of acardius acephalus, acormus, amorphus, anceps, acardiac edema, single umbilical artery, and pump twin risk prediction.

Authors:  Martin J C van Gemert; Michael G Ross; Jeroen P H M van den Wijngaard; Peter G J Nikkels
Journal:  Birth Defects Res       Date:  2021-12-20       Impact factor: 2.661

Review 2.  Intrafetal laser therapy in a monochorionic diamniotic triplet pregnancy with two acardiac fetuses: a case report and literature review.

Authors:  Guiqiong Huang; Hua Liao; Qing Hu; Xiaodong Wang; Haiyan Yu
Journal:  BMC Pregnancy Childbirth       Date:  2021-03-23       Impact factor: 3.007

  2 in total

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