Abstract
Left ventricular noncompaction cardiomyopathy (LVNC) is a rare form of heritable cardiomyopathy with wide genotypic variability, numerous phenotypic variations, and a wide spectrum of clinical disease from asymptomatic to end stage heart failure. Here, we present a case of a 2-year-old boy who presented to their pediatrician with a cough as a first clinical sign of heart failure, rapidly progressing to severe heart failure. He was found to have mixed LVNC with a restrictive phenotype, a rare phenotype of this form of cardiomyopathy. Eventually, the patient was supported via mechanical circulation with a Berlin Heart EXCOR® ventricular assist device as bridge to successful cardiac transplantation. Genetic testing for inherited cardiomyopathies found a mutation in MYH7 (Arg369Gln), known to be associated with various forms of cardiomyopathy, but has not been reported in restrictive LVNC.
Original language | English (US) |
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Journal | OBM Transplantation |
Volume | 4 |
Issue number | 1 |
DOIs | |
State | Published - 2020 |
Keywords
- Cardiomyopathy
- cardiology
- genetics
- pediatric
- transplant
ASJC Scopus subject areas
- Surgery
- Immunology
- Biochemistry, medical
- Transplantation