Abstract

The prevalence of MVP syndrome was determined in 20 boys with clinical, biochemical and electromyographic, and muscle biopsy evidence of DMD. Auscultatory evidence of a non-ejection systolic click, documented by phono, suggested MVP in 7 patients. Echocardiography confirmed MVP in these 7 and in 4 others. Pansystolic, anteriorly concave, posterior motion (> 3 mm beyond CD line) was seen in all patients, abrupt mid-systolic posterior motion in 5, and multiple sequence echoes in 6.

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