Literature DB >> 31512356

Hydrops fetalis in a cohort of 3,137 stillbirths and second trimester miscarriages.

Elizabeth McPherson1.   

Abstract

Hydrops fetalis was diagnosed in 277 (9%) of 3,137 fetuses referred to the Wisconsin Stillbirth Service Program (WiSSP) for etiologic evaluation of stillbirth or second trimester miscarriage. Hydrops was clinically recognized at delivery in only about half the cases, while the remainder were diagnosed at autopsy or during evaluation of records, photographs, and radiographs. The peak incidence of hydrops was at 20-28 weeks. Hydropic fetuses were also frequent before 20 weeks but became increasingly rare toward term. The most frequent identifiable underlying cause was chromosomal (29%), followed by other syndromes (14%), and more distantly by cardiac (6%) and other single system disorders. While the overall prevalence of hydrops and chromosomal causes was comparable to other autopsy series, the frequency of nonchromosomal syndromes was higher, reflecting increased attention to syndrome identification. Lethal multiple pterygium syndrome (LMPS) was identified retrospectively in 17 cases, accounting for 6% of all hydrops; 3/17 had a previous affected sib, emphasizing the importance of accurate diagnosis and counseling. Depending on the underlying cause, hydropic fetuses may be either small (if the cause is chromosomal or LMPS) or large (in cases with other syndromes or cardiac causes) for gestational age. The relatively large number in the "idiopathic" group in WiSSP (104/277; 38%) is probably due to variability of autopsies at local hospitals and limited laboratory data. Improved recognition of hydrops and testing directed at diagnosis of specific underlying causes can lead to improved counseling for families.
© 2019 Wiley Periodicals, Inc.

Entities:  

Keywords:  edema; fetal death; hydrops fetalis; miscarriage; stillbirth

Year:  2019        PMID: 31512356     DOI: 10.1002/ajmg.a.61340

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN: 1552-4825            Impact factor:   2.802


  2 in total

1.  Bi-allelic loss of function variants in SLC30A5 as cause of perinatal lethal cardiomyopathy.

Authors:  Alma Kuechler; Rami Abou Jamra; Johann Kaspar Lieberwirth; Pascal Joset; Anja Heinze; Julia Hentschel; Anja Stein; Antonella Iannaccone; Katharina Steindl
Journal:  Eur J Hum Genet       Date:  2021-02-05       Impact factor: 4.246

2.  Isolated non-immune hydrops fetalis: an observational study on complete spontaneous resolution, perinatal outcome, and long-term follow-up.

Authors:  Sophie Neveling; Alexander Johannes Knippel; Peter Kozlowski
Journal:  Arch Gynecol Obstet       Date:  2022-08-22       Impact factor: 2.493

  2 in total

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