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Rare combination in an infant patient: trisomy 7p and tetralogy of fallot

Published online by Cambridge University Press:  06 September 2022

Osman Guvenc Open the ORCID record for Osman Guvenc [Opens in a new window] ,
Murat Saygi  and
Tugba Akin Duman
Osman Guvenc*
Affiliation:
Department of Pediatric Cardiology, Acibadem Üniversitesi Tip Fakültesi, Istanbul, Turkey
Murat Saygi
Affiliation:
Department of Pediatric Cardiology, Acibadem Üniversitesi Tip Fakültesi, Istanbul, Turkey
Tugba Akin Duman
Affiliation:
Department of Medical Genetics, Haseki Training and Research Hospital, Istanbul, Turkey
*
Author for correspondence: Dr. O. Guvenc, Department of Pediatric Cardiology, Acibadem Üniversitesi Tip Fakültesi, Istanbul, Turkey. Tel: 90 5055013646. E-mail: osmanguvenc1977@gmail.com
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Abstract

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.

Keywords

Trisomy 7ptetralogy of fallotinfant
Type
Brief Report
Information
Cardiology in the Young , First View , pp. 1 - 3
Copyright
© The Author(s), 2022. Published by Cambridge University Press

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