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

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

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

Bibliographic Details
Main Authors: Yannick Hurni, Martina Marangoni, Giulia Garofalo, Marie Cassart, Lisa Tomasi, Isabelle Vandernoot, Guillaume Smits, Caroline Gounongbé
Format: Article
Language:English
Published: Wiley 2021-08-01
Series:Clinical Case Reports
Subjects:
EEC syndrome
fetal medicine
hydrops fetalis
LZTR1 gene
TP63 gene
Online Access:https://doi.org/10.1002/ccr3.4624

Internet

https://doi.org/10.1002/ccr3.4624

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