ISSN 1016-5169 | E-ISSN 1308-4488
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Case Report Holt-Oram Syndrome Associated with the Double Outlet Right Ventricle and Severe Pulmonary Stenosis: Case Report [Turk Kardiyol Dern Ars]
Turk Kardiyol Dern Ars. 1999; 27(2): 124-126

Case Report Holt-Oram Syndrome Associated with the Double Outlet Right Ventricle and Severe Pulmonary Stenosis: Case Report

Özlem M. BOSTAN1, Ergün ÇİL1

Holt-Oraın syndrome is an autosomal dominant disorder, manifesting skeletal malforınation in the upper extreınities, congenital heart defects and cardiac dysrhytmias. A 15-month-old ınale was admitted to pediatric clinic with cyanotic spells. On physical examination, there was radial aplasia of the right arın and aplasia of the right thumb, hypoplasia of the left thumb with hypoplastic thenar eminences. Echocardiography revealed double outlet right ventricle with pulmonary stenosis. Altough multiple forrus of congenital heart diseases and skeletal malformations associated with the HaltOram syndrome have been documented, double outlet right ventricle is rare. Therefore, this case is presented and discussed. Key words

Keywords: Holt-Oram syndrome, double outlet right ventricle.

How to cite this article
Özlem M. BOSTAN, Ergün ÇİL. Case Report Holt-Oram Syndrome Associated with the Double Outlet Right Ventricle and Severe Pulmonary Stenosis: Case Report. Turk Kardiyol Dern Ars. 1999; 27(2): 124-126
Manuscript Language: Turkish


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