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
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

Pagination

1-3

Auteurs

Osman Guvenc (O)

Department of Pediatric Cardiology, Acibadem Üniversitesi Tip Fakültesi, Istanbul, Turkey.

Murat Saygi (M)

Department of Pediatric Cardiology, Acibadem Üniversitesi Tip Fakültesi, Istanbul, Turkey.

Tugba Akin Duman (TA)

Department of Medical Genetics, Haseki Training and Research Hospital, Istanbul, Turkey.

Classifications MeSH