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

Published online by Cambridge University Press:  12 April 2022

Osman Guvenc Open the ORCID record for Osman Guvenc [Opens in a new window] ,
Murat Saygi Open the ORCID record for Murat Saygi [Opens in a new window]  and
Tugba A. Duman Open the ORCID record for Tugba A. Duman [Opens in a new window]
Osman Guvenc*
Affiliation:
Acıbadem University, Medical Faculty, Department of Pediatric Cardiology, Istanbul, Turkey
Murat Saygi
Affiliation:
Acıbadem University, Medical Faculty, Department of Pediatric Cardiology, Istanbul, Turkey
Tugba A. Duman
Affiliation:
Haseki Training and Research Hospital, Department of Medical Genetics, Istanbul, Turkey
*
Author for correspondence: Osman Güvenç, M.D., Merkez Halkalı Mahallesi, Turgut Özal Bulvarı, No:16, Küçükçekmece İstanbul, Turkey. Tel: 0505 5013646 7 02124044444-4286. E-mail: [email protected]
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Abstract

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.

Keywords

Trisomy 7pTetralogy of FallotInfant
Type
Brief Report
Information
Cardiology in the Young , Volume 32 , Issue 12 , December 2022 , pp. 2038 - 2040
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Copyright
© The Author(s), 2022. Published by Cambridge University Press

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