Rare combination in an infant patient: trisomy 7p and 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:
Dec 2022
Historique:
pubmed: 13 4 2022
medline: 16 12 2022
entrez: 12 4 2022
Statut: ppublish

Résumé

This case report presents an infant patient with the association of trisomy 7p and tetralogy of Fallot(ToF). Patients diagnosed with trisomy 7p should certainly be scheduled for an echocardiographic exam and be scanned for any CHD that may accompany it. The CHD that most frequently accompany this syndrome include atrial septal defect, ventricular septal defect, and patent ductus arteriosis. Yet, it should be known that ToF may also be present, albeit rarely.

Identifiants

pubmed: 35411843
pii: S1047951122001044
doi: 10.1017/S1047951122001044
doi:

Types de publication

Case Reports Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

2038-2040

Auteurs

Osman Guvenc (O)

Acıbadem University, Medical Faculty, Department of Pediatric Cardiology, Istanbul, Turkey.

Murat Saygi (M)

Acıbadem University, Medical Faculty, Department of Pediatric Cardiology, Istanbul, Turkey.

Tugba A Duman (TA)

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

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Classifications MeSH