These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


PUBMED FOR HANDHELDS

Search MEDLINE/PubMed


  • Title: [Inclusion-body myositis: a familial report of 3 cases].
    Author: Miró i Andreu O, Fernández-Solá J, Pedrol Clotet E, Coll-Vinent B, Casademont Pou J, Grau Junyent JM, Urbano-Márquez A.
    Journal: Rev Clin Esp; 1994 Nov; 194(11):974-7. PubMed ID: 7846355.
    Abstract:
    Inclusion body myositis (IBM) is a myopathy classified until now within the group of idiopathic inflammatory myopathies (IIM). Nevertheless, its clinical and histological features are specific and different from the other IIM. It is refractory to corticosteroid therapy. Recently, a few cases of IBM with familial transmission have been described, which is the first report in our country; previous reported cases in literature are reviewed. The similarities of some forms of IBM with muscle dystrophies, rather than with inflammatory myopathies are discussed.
    [Abstract] [Full Text] [Related] [New Search]