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Severe coronary artery ectesia in a paediatric patient with Noonan syndrome presenting for transcatheter pulmonary valve placement
Published online by Cambridge University Press: 13 January 2025
Abstract
Coronary ectasia is a very rare phenomenon seen in Noonan syndrome with only a few documented case reports. We describe a 14-year-old with Noonan syndrome and tetralogy of Fallot with described coronary artery ectasia since infancy who presented for possible transcatheter pulmonary valve placement and was found to have severe ectasia of bilateral coronary arteries.
- Type
- Images in Congenital Cardiac Disease
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- © The Author(s), 2025. Published by Cambridge University Press
References
Aniol, CV, Prokop, JW, Rajasekaran, S et al. Dilated coronary arteries in a 2-month-old with RIT1-associated noonan syndrome: a case report. BMC Pediatr 2023; 23: 1.CrossRefGoogle Scholar
Gulati, GS, Gupta, A, Juneja, R, Saxena, A. Ectatic coronary arteries in Noonan syndrome. Tex Heart Inst J 2011; 38: 318–319.Google ScholarPubMed
Uçar, T, Atalay, S, Tekin, M, Tutar, E. Bilateral coronary artery dilatation and supravalvular pulmonary stenosis in a child with noonan syndrome. Pediatr Cardiol 2005; 26: 848–850.CrossRefGoogle Scholar
Calcagni, G, Baban, A, De Luca, E, Leonardi, B, Pongiglione, G, Digilio, MC. Coronary artery ectasia in noonan syndrome: report of an individual with SOS1 mutation and literature review. Am J Med Genet A 2016; 170: 665–669.CrossRefGoogle ScholarPubMed
Loukas, M, Dabrowski, M, Kantoch, M, Ruzyłło, W, Waltenberger, J, Giannikopoulos, P. A case report of noonan’s syndrome with pulmonary valvar stenosis and coronary aneurysms. Med Sci Monit 2004; 10: CS80–CS83.Google ScholarPubMed