A family affected with oculopharygeal muscular dystrophy (OPMD) is reported
. This is an uncommon progressive myopathy. The proband presented for evalu
ation of secretory otitis media with effusion, as a result of tubal dysfunc
tion. CT examination of the father revealed prominent muscular atrophy, and
widespread fatty degeneration of the psoas, paraspinal, gluteal and femora
l muscles. (C) 2001 Published by Elsevier Science Ltd.