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

Clin Case Rep. 2021 Aug 10;9(8):e04624. doi: 10.1002/ccr3.4624. eCollection 2021 Aug.

Authors

Yannick Hurni¹, Martina Marangoni², Giulia Garofalo¹, Marie Cassart^{1

3}, Lisa Tomasi⁴, Isabelle Vandernoot², Guillaume Smits², Caroline Gounongbé¹

Affiliations

¹ Department of Fetal Medicine CHU Saint-Pierre Brussels Belgium.
² Center of Human Genetics Hôpital Erasme Université Libre de Bruxelles Brussels Belgium.
³ Department of Radiology Hôpitaux Iris Sud and CHU Saint-Pierre Brussels Belgium.
⁴ Department of Pediatrics CHU Saint-Pierre Brussels Belgium.

Abstract

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

Keywords: EEC syndrome; LZTR1 gene; TP63 gene; fetal medicine; hydrops fetalis.

© 2021 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd.

Publication types

Case Reports