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A rare coincidence: the long QT syndrome and cardio-facio-cutaneous syndrome

Published online by Cambridge University Press:  08 July 2020

Dilek Giray Open the ORCID record for Dilek Giray [Opens in a new window] ,
Yasemin N. Donmez Open the ORCID record for Yasemin N. Donmez [Opens in a new window] ,
Serdar Epcacan Open the ORCID record for Serdar Epcacan [Opens in a new window]  and
Emine Goktas
Dilek Giray*
Affiliation:
Department of Pediatric Cardiology, Van Training and Research Hospital, Van, Turkey
Yasemin N. Donmez
Affiliation:
Department of Pediatric Cardiology, Van Training and Research Hospital, Van, Turkey
Serdar Epcacan
Affiliation:
Department of Pediatric Cardiology, Van Training and Research Hospital, Van, Turkey
Emine Goktas
Affiliation:
Department of Medical Genetics, Van Training and Research Hospital, Van, Turkey
*
Author for correspondence: Dilek Giray, Department of Pediatric Cardiology, Van Education and Research Hospital, Turkish Republic Ministry of Health, Süphan Mahallesi, Havayolu Kavşağı, Edremit, Van 65300, Turkey. Tel: +90 535 647 8996; Fax: +90 432 2121954. E-mail: [email protected]
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Abstract

Cardio-facio-cutaneous syndrome is a genetic anomaly characterised by craniofacial dysmorphia, developmental retardation, skin lesions, mental retardation/learning disability, and cardiac malformations. Cardio-facio-cutaneous syndrome rarely causes arrhythmias and has not been previously associated with long QT in the literature. With this report, it was aimed to draw attention to a different presentation of the long QT syndrome.

Keywords

Arrhythmiacardio-facio-cutaneous syndromelong QT syndrome
Type
Brief Report
Information
Cardiology in the Young , Volume 30 , Issue 8 , August 2020 , pp. 1209 - 1211
Copyright
© The Author(s), 2020. Published by Cambridge University Press

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