Merged bilateral arterial duct and circumflex retroesophageal right aortic arch in a fetus with normal intracardiac anatomy.
Abortion, Induced
Adult
Anal Canal
/ abnormalities
Aortic Arch Syndromes
/ congenital
Esophagus
/ abnormalities
Female
Fetus
Heart Defects, Congenital
/ pathology
Humans
Kidney
/ abnormalities
Limb Deformities, Congenital
/ pathology
Male
Pulmonary Artery
/ abnormalities
Spine
/ abnormalities
Trachea
/ abnormalities
Bilateral arterial duct
VACTERL
circumflex aortic arch
right aortic arch
Journal
Cardiology in the young
ISSN: 1467-1107
Titre abrégé: Cardiol Young
Pays: England
ID NLM: 9200019
Informations de publication
Date de publication:
Dec 2019
Dec 2019
Historique:
pubmed:
5
11
2019
medline:
21
5
2020
entrez:
5
11
2019
Statut:
ppublish
Résumé
We report the case of a fetus with anamnios sequence and VACTERL syndrome, having a circumflex right aortic arch. Two arterial ducts join anteriorly to form a common vessel that connects to the pulmonary trunk with confluent pulmonary branches. Embryologically, the dorsal right 6th aortic arch did not disappear and the aortic arch development stopped in a symmetrical state with an exceptional "Y-shaped" merged bilateral arterial duct.
Identifiants
pubmed: 31679548
pii: S1047951119002488
doi: 10.1017/S1047951119002488
doi:
Types de publication
Case Reports
Journal Article
Langues
eng
Sous-ensembles de citation
IM