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
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

e04624

Informations 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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Auteurs

Yannick Hurni (Y)

Department of Fetal Medicine CHU Saint-Pierre Brussels Belgium.

Martina Marangoni (M)

Center of Human Genetics Hôpital Erasme Université Libre de Bruxelles Brussels Belgium.

Giulia Garofalo (G)

Department of Fetal Medicine CHU Saint-Pierre Brussels Belgium.

Marie Cassart (M)

Department of Fetal Medicine CHU Saint-Pierre Brussels Belgium.
Department of Radiology Hôpitaux Iris Sud and CHU Saint-Pierre Brussels Belgium.

Lisa Tomasi (L)

Department of Pediatrics CHU Saint-Pierre Brussels Belgium.

Isabelle Vandernoot (I)

Center of Human Genetics Hôpital Erasme Université Libre de Bruxelles Brussels Belgium.

Guillaume Smits (G)

Center of Human Genetics Hôpital Erasme Université Libre de Bruxelles Brussels Belgium.

Caroline Gounongbé (C)

Department of Fetal Medicine CHU Saint-Pierre Brussels Belgium.

Classifications MeSH