{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,30]],"date-time":"2026-09-30T01:29:02Z","timestamp":1790731742049,"version":"4.1.0"},"reference-count":19,"publisher":"SAGE Publications","issue":"6","license":[{"start":{"date-parts":[[2020,11,1]],"date-time":"2020-11-01T00:00:00Z","timestamp":1604188800000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/journals.sagepub.com\/page\/policies\/text-and-data-mining-license"}],"funder":[{"name":"Jack Long's Gift"}],"content-domain":{"domain":["journals.sagepub.com"],"crossmark-restriction":true},"short-container-title":["World J Pediatr Congenit Heart Surg"],"published-print":{"date-parts":[[2020,11]]},"abstract":"<jats:p>\n                    Ebstein anomaly has a breadth of presentations, including \u201ctypical\u201d and \u201catypical,\u201d and can be confused with congenital tricuspid dysplasia. We summarize how to differentiate within this spectrum of disease. Both typical and atypical Ebstein have an underlying failure of delamination, but atypical Ebstein does not have \u22658mm\/m\n                    <jats:sup>2<\/jats:sup>\n                    apical septal leaflet displacement. In congenital tricuspid dysplasia, delamination is normal, while the leaflets and subvalvar apparatus are abnormal. To summarize, the sine qua non feature of Ebstein anomaly, present in both typical and atypical, is the failure of delamination. These are distinct from congenital tricuspid valve dysplasia in which the pathology is in the leaflet itself.\n                  <\/jats:p>","DOI":"10.1177\/2150135120949235","type":"journal-article","created":{"date-parts":[[2020,11,8]],"date-time":"2020-11-08T13:40:36Z","timestamp":1604842836000},"page":"783-791","update-policy":"https:\/\/doi.org\/10.1177\/sage-journals-update-policy","source":"Crossref","is-referenced-by-count":32,"title":["The Congenital Tricuspid Valve Spectrum: From Ebstein to Dysplasia"],"prefix":"10.1177","volume":"11","author":[{"given":"Elizabeth H.","family":"Stephens","sequence":"first","affiliation":[{"name":"Department of Cardiovascular Surgery, Mayo Clinic, Rochester, MN, USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Joseph A.","family":"Dearani","sequence":"additional","affiliation":[{"name":"Department of Cardiovascular Surgery, Mayo Clinic, Rochester, MN, USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Muhammad Y.","family":"Qureshi","sequence":"additional","affiliation":[{"name":"Division of Pediatric Cardiology, Mayo Clinic, Rochester, MN, USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Naser","family":"Ammash","sequence":"additional","affiliation":[{"name":"Department of Cardiovascular Diseases, Mayo Clinic, Rochester, MN, USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Joseph J.","family":"Maleszewski","sequence":"additional","affiliation":[{"name":"Department of Pathology, Mayo Clinic, Rochester, MN, USA"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"179","published-online":{"date-parts":[[2020,11,8]]},"reference":[{"key":"bibr1-2150135120949235","first-page":"238","author":"Ebstein W","year":"1866","journal-title":"Arch Anat Physiol Wissensch Med"},{"key":"bibr2-2150135120949235","volume-title":"The Clinical Recognition of Congenital Heart 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