1. [Hereditary inclusion-body myopathy].
- Author
-
Kucharz EJ
- Subjects
- Humans, Myositis, Inclusion Body classification, Myositis, Inclusion Body diagnosis, Myositis, Inclusion Body genetics
- Abstract
Hereditary inclusion-body myopathy (h-IBM) is a heterogeneous group of disorders characterized by progressive weakness of some skeletal muscles and pathological feature, intercellular rimmed vacuoles in the muscular filaments. h-IBM is not associated with inflammatory infiltrations and term myopathy is used as opposite to spontaneous inclusion-body myositis. h-IBM is classified into autosomal recessive and autosomal dominant subgroups.
- Published
- 1999