AI Article Synopsis
- - A 14-year-old Caucasian male was uniquely diagnosed with arrhythmogenic right ventricular dysplasia (ARVD) alongside long QT syndrome (LQTS).
- - Genetic testing confirmed the presence of both ARVD and LQTS in the patient.
- - This case of having both ARVD and LQTS together is a rare occurrence that has not been previously documented in medical literature.
Article Abstract
We describe a unique presentation of arrhythmogenic right ventricular dysplasia (ARVD) in a 14-year-old Caucasian male who was additionally diagnosed with long QT syndrome (LQTS). Genetic testing eventually confirmed the diagnosis of both ARVD and LQTS, which combined, to our knowledge, has not been reported in the literature.
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| http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6932431 | PMC |
| http://dx.doi.org/10.1111/anec.12043 | DOI Listing |
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