-transparent.png){kind=logo}
A 75-year-old French-Canadian woman with familial oculopharyngeal dystrophy demonstrated histopathologic alterations similar to those of idiopathic polymyositis. A second biopsy obtained 15 months later was more consistent with previously reported cases. It is suggested that certain patients with oculopharyngeal dystrophy may pass through an initial phase of secondary muscle inflammation similar to that seen in some other heritable myopathies.
Related Publications
E P Bosch, and
J D Gowans, and
T Munsat
January 2001,
Ryoikibetsu shokogun shirizu,
E P Bosch, and
J D Gowans, and
T Munsat
January 2017,
Brazilian journal of otorhinolaryngology,
E P Bosch, and
J D Gowans, and
T Munsat
January 2009,
Current neurology and neuroscience reports,
E P Bosch, and
J D Gowans, and
T Munsat
January 1978,
Revue de laryngologie - otologie - rhinologie,
E P Bosch, and
J D Gowans, and
T Munsat
January 1982,
Acta neuropathologica,
E P Bosch, and
J D Gowans, and
T Munsat
January 2012,
Neurobiology of disease,
E P Bosch, and
J D Gowans, and
T Munsat
July 1981,
Archives of internal medicine,
E P Bosch, and
J D Gowans, and
T Munsat
November 1990,
Neurologia (Barcelona, Spain),
E P Bosch, and
J D Gowans, and
T Munsat
April 1998,
Neuromuscular disorders : NMD,
E P Bosch, and
J D Gowans, and
T Munsat
December 1982,
Acta neurologica,
