Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/32704
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dc.contributor.authorSchrapnel, M.-
dc.contributor.authorGoyert, S.-
dc.contributor.authorByard, R.-
dc.date.issued2001-
dc.identifier.citationMedicine Science and the Law, 2001; 41(2):159-162-
dc.identifier.issn0025-8024-
dc.identifier.issn2042-1818-
dc.identifier.urihttp://hdl.handle.net/2440/32704-
dc.description.abstractA 32-year-old man who died suddenly and unexpectedly was found at autopsy to have prominent fatty infiltration of his left ventricle with fibrous scarring, in the presence of normal coronary arteries, The right ventricle was minimally involved. A diagnosis of ventricular dysplasia largely limited to the left ventricle was made. Subsequent family screening identified a brother with clinical manifestations of ventricular dysplasia. This case provides further evidence for the association of left ventricular dysplasia with sudden death, and demonstrates that left ventricular involvement may also be inheritable. Whether predominantly left ventricular dysplasia is a manifestation of right ventricular dysplasia, or is a separate entity, is yet to be determined.-
dc.description.statementofresponsibilityShrapnel, M.; Gilbert, J. D.; Byard, R. W.-
dc.language.isoen-
dc.publisherChiltern Publishing-
dc.source.urihttp://dx.doi.org/10.1177/002580240104100213-
dc.subjectHeart Ventricles-
dc.subjectHumans-
dc.subjectHeart Defects, Congenital-
dc.subjectArrhythmogenic Right Ventricular Dysplasia-
dc.subjectDeath, Sudden-
dc.subjectAdult-
dc.subjectMale-
dc.subjectArrhythmias, Cardiac-
dc.title'Arrhythmogenic left ventricular dysplasia' and sudden death-
dc.typeJournal article-
dc.identifier.doi10.1177/002580240104100213-
pubs.publication-statusPublished-
dc.identifier.orcidByard, R. [0000-0002-0524-5942]-
Appears in Collections:Aurora harvest
Pathology publications

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