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
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