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April 1, 1983HeartOpen Access

Asymmetric septal hypertrophy and hypertrophic cardiomyopathy.

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Authors

RER EmanuelBoston University JMJ MarcomichelakisMiddlesex Hospital RWR WithersUniversity Hospital of Wales

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Implication

May warrant screening relatives of HCM patients; leaves open inheritance patterns and penetrance in larger cohorts.

Key Points

Key points are not available for this paper at this time.

Cite This Study

Emanuel et al. (1983) studied this question.

synapsesocial.com/papers/6a964fb3dbc641e6a0a6b33a https://doi.org/10.1136/hrt.49.4.309

Topics

Echocardiography Hypertrophic cardiomyopathy

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Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

1Asymmetric septal hypertrophy in a large Amish kindred1975 · 2 citations
2Congenitally bicuspid aortic valves. Clinicogenetic study of 41 families.1978 · 94 citations
3Prevalence and characteristics of disproportionate ventricular septal thickening in patients with acquired or congenital heart diseases: echocardiographic and morphologic findings.1977 · 88 citations
4Differences in Distribution of Myocardial Abnormalities in Patients with Obstructive and Nonobstructive Asymmetric Septal Hypertrophy (ASH)1974 · 184 citations
5Asymmetric septal hypertrophy and myocardial fiber disarray. Features of normal, developing, and malformed hearts.1977 · 109 citations