Spontaneous resolution of nonimmune hydrops fetalis in a fetus with TP63 gene mutation and LZTR1 gene variants

Yannick Hurni; Martina Marangoni; Giulia Garofalo; Marie Cassart; Lisa Tomasi; Isabelle Vandernoot; Guillaume Smits; Caroline Gounongbé

doi:10.1002/ccr3.4624

Clinical Case Reports (Aug 2021)

Spontaneous resolution of nonimmune hydrops fetalis in a fetus with TP63 gene mutation and LZTR1 gene variants

Yannick Hurni,
Martina Marangoni,
Giulia Garofalo,
Marie Cassart,
Lisa Tomasi,
Isabelle Vandernoot,
Guillaume Smits,
Caroline Gounongbé

Affiliations

Yannick Hurni: Department of Fetal Medicine CHU Saint‐Pierre Brussels Belgium
Martina Marangoni: Center of Human Genetics Hôpital ErasmeUniversité Libre de Bruxelles Brussels Belgium
Giulia Garofalo: Department of Fetal Medicine CHU Saint‐Pierre Brussels Belgium
Marie Cassart: Department of Fetal Medicine CHU Saint‐Pierre Brussels Belgium
Lisa Tomasi: Department of Pediatrics CHU Saint‐Pierre Brussels Belgium
Isabelle Vandernoot: Center of Human Genetics Hôpital ErasmeUniversité Libre de Bruxelles Brussels Belgium
Guillaume Smits: Center of Human Genetics Hôpital ErasmeUniversité Libre de Bruxelles Brussels Belgium
Caroline Gounongbé: Department of Fetal Medicine CHU Saint‐Pierre Brussels Belgium

DOI: https://doi.org/10.1002/ccr3.4624
Journal volume & issue: Vol. 9, no. 8
pp. n/a – n/a

Abstract

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Abstract In cases of fetal hydrops, searching for an etiology is essential to evaluate the fetal prognosis and propose the most appropriate management.

Published in Clinical Case Reports

ISSN: 2050-0904 (Online)
Publisher: Wiley
Country of publisher: United Kingdom
LCC subjects: Medicine: Medicine (General)
Website: https://onlinelibrary.wiley.com/journal/20500904

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Abstract

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