Rare combination in an infant patient: trisomy 7p and tetralogy of fallot.
Trisomy 7p
infant
tetralogy of fallot
Journal
Cardiology in the young
ISSN: 1467-1107
Titre abrégé: Cardiol Young
Pays: England
ID NLM: 9200019
Informations de publication
Date de publication:
06 Sep 2022
06 Sep 2022
Historique:
entrez:
6
9
2022
pubmed:
7
9
2022
medline:
7
9
2022
Statut:
aheadofprint
Résumé
This case report presents an infant patient with the association of trisomy 7p and tetralogy of fallot (TEF). Patients diagnosed with trisomy 7p should certainly be scheduled for an echocardiographic exam and be scanned for any CHDs that may accompany it. The CHDs that most frequently accompany this syndrome include atrial septal defect, ventricular septal defect, and patent ductus arteriosis. Yet, it should be known that TEF may also be present, albeit rarely.
Identifiants
pubmed: 36065713
pii: S1047951122002062
doi: 10.1017/S1047951122002062
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM