Variable phenotypic expression of Apert syndrome in monozygotic twins.
Apert syndrome
congenital diaphragmatic hernia
craniosynostosis
fetal autopsy
fetal ultrasound
monozygotic twins
Journal
Clinical case reports
ISSN: 2050-0904
Titre abrégé: Clin Case Rep
Pays: England
ID NLM: 101620385
Informations de publication
Date de publication:
Jan 2019
Jan 2019
Historique:
received:
02
08
2018
revised:
11
09
2018
accepted:
20
10
2018
entrez:
19
1
2019
pubmed:
19
1
2019
medline:
19
1
2019
Statut:
epublish
Résumé
Apert syndrome in monozygotic twins can lead to different phenotypic expression of the disease in the two fetuses. Apert syndrome can be associated with congenital left diaphragmatic hernia and cleft palate.
Identifiants
pubmed: 30656008
doi: 10.1002/ccr3.1915
pii: CCR31915
pmc: PMC6333066
doi:
Types de publication
Case Reports
Langues
eng
Pagination
54-57Références
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