{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,14]],"date-time":"2026-08-14T17:29:53Z","timestamp":1786728593234,"version":"build-2736575974"},"reference-count":15,"publisher":"Ovid Technologies (Wolters Kluwer Health)","issue":"3","license":[{"start":{"date-parts":[[2025,7,1]],"date-time":"2025-07-01T00:00:00Z","timestamp":1751328000000},"content-version":"unspecified","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by-nc-sa\/4.0"}],"content-domain":{"domain":["lww.com","ovid.com"],"crossmark-restriction":true},"short-container-title":[],"published-print":{"date-parts":[[2025,7]]},"abstract":"<jats:title>Abstract<\/jats:title>\n                  <jats:p>Tuberous sclerosis complex has an autosomal dominant pattern of inheritance. Hamartomas are seen in various organs in tuberous sclerosis. Tuberous sclerosis is linked to cardiac rhabdomyomas, which is one of the common heart tumors in children. We present a full-term neonate who was suspected to have the congenital disease due to the presence of pansystolic murmur on examination. Echocardiography revealed multiple rhabdomyomas in the right ventricular (RV) and LV wall and interventricular septum of varying sizes and shapes. The largest rhabdomyoma arising from the lateral wall of RV measuring 16 mm \u00d7 18 mm. There was 6 mm \u00d7 8 mm rhabdomyoma protruding in the left ventricular outflow tract in nonobstructive manner. There was no inflow or outflow obstruction. Small apical muscular ventricular septal defect noted. Mother had numerous papulonodular lesions on both cheeks, nose, and forehead (adenoma sebaceum). No other neurocutaneous markers were present. Mother had no systemic involvement. In babies born to mothers with suspected tuberous sclerosis, a high degree of suspicion is required to rule out cardiac tumors.<\/jats:p>","DOI":"10.4103\/jcecho.jcecho_5_25","type":"journal-article","created":{"date-parts":[[2025,10,1]],"date-time":"2025-10-01T05:00:41Z","timestamp":1759294841000},"page":"289-291","update-policy":"https:\/\/doi.org\/10.1097\/lww.0000000000001000","source":"Crossref","is-referenced-by-count":2,"title":["Cardiac Rhabdomyoma in a Neonate"],"prefix":"10.4103","volume":"35","author":[{"given":"Chandrakant M.","family":"Bokade","sequence":"first","affiliation":[{"name":"Department of Pediatric, Datta Meghe Medical College, Datta Meghe Institute of Higher Education and Research, Nagpur, Maharashtra, India"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Nisha R.","family":"Aglave","sequence":"additional","affiliation":[{"name":"Department of Pediatric, Datta Meghe Medical College, Datta Meghe Institute of Higher Education and Research, Nagpur, Maharashtra, India"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Milind M.","family":"Suryawanshi","sequence":"additional","affiliation":[{"name":"Department of Pediatric, Indira Gandhi Government Medical College, Nagpur, Maharashtra, India"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"276","published-online":{"date-parts":[[2025,9,29]]},"reference":[{"key":"R1-20251010","first-page":"12","article-title":"Previously undiagnosed tuberous sclerosis complex in a newborn: A case report","volume":"3","author":"Coskun","year":"2017","journal-title":"J Rare Disord Diagn Ther"},{"key":"R2-20251010","doi-asserted-by":"crossref","first-page":"332","DOI":"10.3390\/genes15030332","article-title":"The genetics of tuberous sclerosis complex and related mtoropathies: Current understanding and future directions","volume":"15","author":"Man","year":"2024","journal-title":"Genes"},{"key":"R3-20251010","doi-asserted-by":"crossref","first-page":"619","DOI":"10.1177\/088307389801301205","article-title":"Tuberous sclerosis complex and neonatal seizures","volume":"13","author":"Miller","year":"1998","journal-title":"J Child Neurol"},{"key":"R4-20251010","doi-asserted-by":"crossref","first-page":"487","DOI":"10.1016\/S0002-9149(03)00677-5","article-title":"Association between cardiac tumors and tuberous sclerosis in the fetus and neonate","volume":"92","author":"Tworetzky","year":"2003","journal-title":"Am J Cardiol"},{"key":"R5-20251010","doi-asserted-by":"crossref","first-page":"516","DOI":"10.1016\/0735-1097(95)80031-B","article-title":"Diagnosis and management of fetal cardiac tumors: A multicenter experience and review of published reports","volume":"26","author":"Holley","year":"1995","journal-title":"J Am Coll Cardiol"},{"key":"R6-20251010","doi-asserted-by":"crossref","first-page":"584","DOI":"10.1136\/hrt.72.6.584","article-title":"Cardiac involvement in tuberous sclerosis","volume":"72","author":"M\u00fchler","year":"1994","journal-title":"Br Heart J"},{"key":"R7-20251010","first-page":"8395260","article-title":"Spontaneous regression of cardiac rhabdomyoma presenting as severe left ventricular inlet obstruction in a neonate with tuberous sclerosis","author":"Song","year":"2018","journal-title":"Case Rep Cardiol 2018"},{"key":"R8-20251010","doi-asserted-by":"crossref","first-page":"825","DOI":"10.1002\/1097-0142(19850815)56:4<825::AID-CNCR2820560421>3.0.CO;2-7","article-title":"Primary and secondary tumors of childhood involving the heart, pericardium, and great vessels. 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