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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.
Autores principales: | Hurni, Yannick, Marangoni, Martina, Garofalo, Giulia, Cassart, Marie, Tomasi, Lisa, Vandernoot, Isabelle, Smits, Guillaume, Gounongbé, Caroline |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
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 |
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