Spontaneous resolution of nonimmune hydrops fetalis in a fetus with
EEC syndrome
LZTR1 gene
TP63 gene
fetal medicine
hydrops fetalis
Journal
Clinical case reports
ISSN: 2050-0904
Titre abrégé: Clin Case Rep
Pays: England
ID NLM: 101620385
Informations de publication
Date de publication:
Aug 2021
Aug 2021
Historique:
received:
14
04
2021
revised:
23
06
2021
accepted:
06
07
2021
entrez:
17
8
2021
pubmed:
18
8
2021
medline:
18
8
2021
Statut:
epublish
Résumé
In cases of fetal hydrops, searching for an etiology is essential to evaluate the fetal prognosis and propose the most appropriate management.
Identifiants
pubmed: 34401172
doi: 10.1002/ccr3.4624
pii: CCR34624
pmc: PMC8353418
doi:
Types de publication
Case Reports
Langues
eng
Pagination
e04624Informations de copyright
© 2021 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd.
Déclaration de conflit d'intérêts
None declared.
Références
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