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Apical hypertrophic cardiomyopathy with subendocardial late gadolinium enhancement in an adolescent

Published online by Cambridge University Press:  30 December 2020

Simona Boroni Grazioli Open the ORCID record for Simona Boroni Grazioli [Opens in a new window] ,
Marc-Philip Hitz  and
Inga Voges
Simona Boroni Grazioli
Affiliation:
Department of Congenital Heart Disease and Pediatric Cardiology, University Hospital Schleswig-Holstein, Kiel, Germany
Marc-Philip Hitz
Affiliation:
Department of Congenital Heart Disease and Pediatric Cardiology, University Hospital Schleswig-Holstein, Kiel, Germany Department for Human Genetics, University Hospital Schleswig-Holstein, Kiel, Germany
Inga Voges*
Affiliation:
Department of Congenital Heart Disease and Pediatric Cardiology, University Hospital Schleswig-Holstein, Kiel, Germany
*
Author for correspondence: Dr Inga Voges. Department of Congenital Heart Disease and Pediatric Cardiology, Arnold-Heller-Str. 3, Haus 9, University Hospital Schleswig-Holstein, Campus Kiel. Tel: +49(0)43150025602; Fax: +49(0)43150025604. E-mail: [email protected]
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Abstract

A 17-year-old boy with a history of dyspnea attacks and chest pain was referred to our paediatric cardiology department. Electrocardiogram at presentation showed T-wave inversion in the inferior leads. Cardiovascular magnetic resonance imaging revealed the rare diagnosis of apical hypertrophic cardiomyopathy with subendocardial late gadolinium enhancement, missed by echocardiography.

Keywords

Pediatric cardiomyopathycardiovascular magnetic resonancegenetics
Type
Images in Congenital Cardiac Disease
Information
Cardiology in the Young , Volume 31 , Issue 2 , February 2021 , pp. 286 - 288
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Copyright
© The Author(s), 2020. Published by Cambridge University Press

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References

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