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Left Ventricular Non-compaction in Holt-Oram Syndrome.
- Source :
-
Heart, lung & circulation [Heart Lung Circ] 2016 Jun; Vol. 25 (6), pp. 626-30. Date of Electronic Publication: 2016 Jan 28. - Publication Year :
- 2016
-
Abstract
- Holt-Oram Syndrome is an autosomal dominant condition with complete penetrance and which involves upper limb skeletal and cardiac abnormalities. The latter can be structural defects or involve the conduction system. This report details the occurrence of left ventricular non-compaction in multiple family members with Holt-Oram Syndrome. It is recommended that patients with the Holt-Oram Syndrome be considered for comprehensive cardiac evaluation to exclude non-compaction cardiomyopathy as this may have significant prognostic implications.<br /> (Copyright © 2016 Australian and New Zealand Society of Cardiac and Thoracic Surgeons (ANZSCTS) and the Cardiac Society of Australia and New Zealand (CSANZ). Published by Elsevier B.V. All rights reserved.)
- Subjects :
- Adult
Humans
Male
Abnormalities, Multiple physiopathology
Cardiomyopathies physiopathology
Heart Defects, Congenital physiopathology
Heart Septal Defects, Atrial physiopathology
Heart Ventricles physiopathology
Lower Extremity Deformities, Congenital physiopathology
Upper Extremity Deformities, Congenital physiopathology
Subjects
Details
- Language :
- English
- ISSN :
- 1444-2892
- Volume :
- 25
- Issue :
- 6
- Database :
- MEDLINE
- Journal :
- Heart, lung & circulation
- Publication Type :
- Academic Journal
- Accession number :
- 26874791
- Full Text :
- https://doi.org/10.1016/j.hlc.2015.12.098