Congenital heart malformations associated with disproportionate ventricular septal thickening.
- 1 November 1975
- journal article
- abstracts
- Published by Wolters Kluwer Health in Circulation
- Vol. 52 (5) , 926-932
- https://doi.org/10.1161/01.cir.52.5.926
Abstract
Asymmetric septal hypertrophy, or ASH, is a genetically determined myocardial disorder that is transmitted as an autosomal dominant trait. ASH is characterized by a disproportionately thickened ventricular septum that contains numerous hypertrophied, bizarrely-shaped and disorganized cardiac muscle cells. Disproportionate hypertrophy of the ventricular septum has also been observed in association with certain congenital cardiac malformations. To determine whether such congenital cardiac malformations are part of the disease spectrum of genetically determined ASH, cardiac pathologic observations were made in eight patients with disproportionate septal thickening (ventricular septal to posterobasal left ventricular free wall thickness ratios of 1.5 to 2.5) and the following three categories of associated lesions: 1) parachute deformity of the mitral valve (occurring either as an isolated lesion or with ventricular septal defect, coarctation of the aorta, supravalvular ring of the left atrium, or double outlet right ventricle); 2) complete interruption of the aortic arch; and 3) ventricular septal defect. The arrangement of cardiac muscle cells in the disproportionately thickened ventricular septum was normal in six of the eight patients; in the other two patients (one with parachute deformity of the mitral valve and one with ventricular septal defect) numerous bundles of hypertrophied cardiac muscle cells were interlaced in a disorganized fashion among more normally arranged bundles of cells. First degree relatives of six of the eight patients were studied by echocardiography and found to have normal ventricular wall thicknesses and septal-free wall ratios. It is concluded that disproportionate ventricular septal thickening may occur in patients with a variety of congenital heart malformations, but that such a finding is not necessarily a manifestation of the disease spectrum of genetically determined ASH.Keywords
This publication has 25 references indexed in Scilit:
- Differences in Distribution of Myocardial Abnormalities in Patients with Obstructive and Nonobstructive Asymmetric Septal Hypertrophy (ASH)Circulation, 1974
- Echocardiographic features of primary pulmonary hypertensionThe American Journal of Cardiology, 1974
- Coexistent fixed congenital and idiopathic hypertrophic subaortic stenosisThe American Journal of Cardiology, 1973
- Congenital idiopathic hypertrophic subaortic stenosis associated with a phenotypic Turner's syndromeThe American Journal of Cardiology, 1972
- Friedreich's ataxia associated with idiopathic hypertrophic subaortic stenosisAmerican Heart Journal, 1972
- Hypertrophic obstructive cardiomyopathy and Friedreich's ataxiaThe American Journal of Cardiology, 1971
- The developmental complex of “parachute mitral valve,” supravalvular ring of left atrium, subaortic stenosis, and coarctation of aortaPublished by Elsevier ,1963
- Common A-V orifice with pulmonary valvular and hypertrophic subaortic stenosisThe American Journal of Cardiology, 1962
- Biventricular origin of the pulmonary trunk with subaortic stenosis above the ventricular septal defectAmerican Heart Journal, 1961
- A complex of congenital cardiac anomalies: Ventricular septal defect, biventricular origin of the pulmonary trunk, and subaortic stenosisAmerican Heart Journal, 1955