We report a case of late onset of Becker's muscular dystrophy (BMD), diagno
sed at the age of 60, which showed a very mild clinical course. Remarkably,
the immunohistochemical pattern did not show significant alterations, whil
e Western blotting disclosed low molecular weight dystrophin. DNA analysis
showed a deletion of the exons 45 - 53 of the Xp21 gene, which is fairly ty
pical of Becker's muscular dystrophy but not predictable of clinical course
. The possibility of Xp21 muscular dystrophy must be considered in all myop
athies of uncertain cause, also in elderly patients.