We report an unusual example of Becker muscular dystrophy in which the
patient was asymptomatic until his mid-60s, and diagnosis was not mad
e until he was 67 years old. The patient had the unusual deletion of e
xons 3 to 9 within an actin-binding region of the dystrophin gene, rem
oval or disruption of which is almost invariably associated with a mor
e severe clinical phenotype. Our case illustrates the danger of drawin
g conclusions about possibly symptomatic deletions without lifelong fo
llow-up.