Phospholamban Cardiomyopathy Leading to Advanced Heart Failure in an Active Duty Service Member
A phospholamban mutation is a rare genetic cause of dilated cardiomyopathy (DCM). Our case describes a young service member who presented with advanced heart failure and was found to have a familial DCM from an autosomal dominant phospholamban mutation. He ultimately underwent a successful heart transplant just 23 days after his initial presentation. This case highlights the importance of genetic screening and surveillance for patients with a family history of DCM, and it identifies a gap in medical standards for military accession.
Authors
- Satoshi R. Shin
- Luke Oakley (ORCID: https://orcid.org/0000-0001-9299-7319)
- Robert N Geis (ORCID: https://orcid.org/0000-0002-5297-9789)
- Dylan Wessman
- Anthony Choi (ORCID: https://orcid.org/0000-0002-0499-3279)
- Ryan Choi (ORCID: https://orcid.org/0000-0003-4877-6871)
Institutions
- Naval Medical Center San Diego (US)
Publication Details
- Journal
- Military Medicine
- Published
- 2024-08-23
- DOI
- https://doi.org/10.1093/milmed/usae396
- Primary Topic
- Cardiovascular Effects of Exercise
- Type
- article
- Field-Weighted Citation Impact
- 0.00