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

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

Detalles Bibliográficos
Autores principales: Hurni, Yannick, Marangoni, Martina, Garofalo, Giulia, Cassart, Marie, Tomasi, Lisa, Vandernoot, Isabelle, Smits, Guillaume, Gounongbé, Caroline
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Case Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8353418/
https://www.ncbi.nlm.nih.gov/pubmed/34401172
http://dx.doi.org/10.1002/ccr3.4624

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8353418/
https://www.ncbi.nlm.nih.gov/pubmed/34401172
http://dx.doi.org/10.1002/ccr3.4624

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