Only a limited number of families with clear monogenic inheritance of nonsyndromic forms of congenital valve defects have been described. We describe two multiplex pedigrees with a similar nonsyndromic form of heart valve anomalies that segregate as an autosomal dominant condition. The first family is a three-generation pedigree with 10 family members affected with congenital defects of the cardiac valves, including six patients with aortic stenosis and/or aortic regurgitation. Pulmonary and/or tricuspid valve abnormalities were present in three patients, and ventricular septal defect (VSD) was present in two patients. The second family consists of 11 patients in three generations with aortic valve stenosis in seven patients, defects of the pulmonary valves in two patients, and atrial septal defect (ASD) in two patients. Incomplete penetrance was observed in both families. Although left-ventricular outflow tract obstruction was present in most family members, the co-occurrence with pulmonary valve abnormalities and septal defects in both families is uncommon. These families provide evidence that left-sided obstructive defects and thoracic aortic aneurysm may be accompanied by right-sided defects, and even septal defects. These families might be instrumental in identifying genes involved in cardiac valve morphogenesis and malformation.

Additional Metadata
Keywords Aortic dilatation, Autosomal dominant, Bicuspid aortic valve, Candidate genes, Congenital heart malformation, Heart valves, Left-ventricular outflow tract obstruction, Pathways, Thoracic aortic aneurysm, adult, aorta stenosis, aorta valve prosthesis, aorta valve regurgitation, aorta valve stenosis, article, autosomal dominant inheritance, bicuspid aortic valve, child, clinical article, clinical feature, congenital heart malformation, controlled study, female, heart atrium septum defect, heart left ventricle failure, heart murmur, heart ventricle septum defect, human, male, mitral valve prosthesis, mitral valve regurgitation, mitral valve stenosis, newborn, priority journal, pulmonary valve atresia, pulmonary valve disease, pulmonary valve insufficiency, school child, tricuspid valve regurgitation, valvular heart disease
Persistent URL,
Journal American Journal of Medical Genetics. Part A
Wessels, M.W, van de Laar, I.M.B.H, Roos-Hesselink, J.W, Strikwerda, S, Majoor-Krakauer, D.F, de Vries, B.B.A, … Willems, P.J. (2009). Autosomal dominant inheritance of cardiac valves anomalies in two families: Extended spectrum of left-ventricular outflow tract obstruction. American Journal of Medical Genetics. Part A, 149(2), 216–225. doi:10.1002/ajmg.a.32594