A Novel Heterozygous Desmoplakin Variant Causes Cardiocutaneous Syndrome with Arrhythmogenic Cardiomyopathy and Palmoplantar Keratosis

Author:

Çimen Tolga1ORCID,Medeiros-Domingo Argelia2ORCID,Kolios Antonios3,Akdiş Deniz1,Anwer Shehab1ORCID,Tanner Felix C.1,Brunckhorst Corinna1,Duru Firat14ORCID,Saguner Ardan M.1ORCID

Affiliation:

1. Department of Cardiology, University Heart Center, University Hospital Zurich, 8091 Zurich, Switzerland

2. Swiss DNAlysis Laboratory, 8600 Dubendorf, Switzerland

3. Department of Dermatology, University Hospital Zurich, 8091 Zurich, Switzerland

4. Center for Integrative Human Physiology (ZIHP), University of Zurich, 8057 Zurich, Switzerland

Abstract

Cardiocutaneous syndrome (CCS) is often caused by genetic variants in desmoplakin (DSP) in the presence of thick calluses on the hands and soles of the feet (palmoplantar keratoderma) in combination with arrhythmogenic cardiomyopathy. In this case report, we describe a 58-year-old man presenting with a history of cardiomyopathy with recurrent sustained ventricular tachycardia and palmoplantar keratosis. The cardiological evaluation showed biventricular cardiomyopathy, and repeated genetic testing identified a novel DSP variant. Repeated genetic testingis clinically meaningful in patients with a high probability of a specific inherited cardiac disease, such as CCS, particularly if molecular screening has been performed in the pre-NGS era with an incomplete NGS panel or outdated technology as presented in this case report.

Funder

Georg und Bertha Schwyzer-Winiker Foundation

Swiss National Science Foundation

Publisher

MDPI AG

Subject

General Medicine

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