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Barlow syndrome

A genetically heterogeneous hereditary form of mitral valve prolapse that appears to be inherited as an autosomal dominant or x-linked trait and exhibits both sex- and age-dependent PENETRANCE. OMIM: 157700
Also Known As:
Mitral regurgitation, familial; Mitral valve prolapse, familial, X-linked; Myxomatous valvular disease, familial
Networked: 1 relevant articles (0 outcomes, 0 trials/studies)

Disease Context: Research Results

Related Diseases

1. Prolapse

Experts

1. Borger, Michael A: 1 article (01/2010)
2. Mohr, Friedrich W: 1 article (01/2010)

Therapies and Procedures

1. Thoracotomy