encyclopedia of medical concepts
ψ 
ψ 

Myositis, Inclusion Body

More information in Books or onNLM PubMed
Definition: Progressive myopathies characterized by the presence of inclusion bodies on muscle biopsy. Sporadic and hereditary forms have been described. The sporadic form is an acquired, adult-onset inflammatory vacuolar myopathy affecting proximal and distal muscles. Familial forms usually begin in childhood and lack inflammatory changes. Both forms feature intracytoplasmic and intranuclear inclusions in muscle tissue. (Adams et al., Principles of Neurology, 6th ed, pp1409-10)  do not coord with INCLUSION BODIES but coord with INCLUSION BODIES, VIRAL if relevant (IM or NIM)    Other names Myositides, Inclusion Body; Inclusion Body Myositides; Sporadic Inclusion Body Myositis; Myositis, Inclusion Body, Sporadic; Inclusion Body Myositis, Sporadic; Inclusion Body Myopathy, Sporadic; Myopathy, Inclusion Body, Sporadic; Inclusion Body Myositis
 
SubstanceCAS Registry & nameCategoriesSource
Inclusion body myopathy, autosomal dominant  0   *Contracture/congenital *Ophthalmoplegia *Myositis, Inclusion Body/congenital.
Inclusion body myopathy autosomal recessive  0   *Myositis, Inclusion Body/congenital.
Myopathy, desmin storage  0   *Myositis, Inclusion Body.

To share this definition, click "text" (Facebook, Twitter) or "link" (blog, mail) then paste text link
Ads by Google

Sources: NLM Medical Subject Headings, NIH UMLS, Drugs@FDA, FDA AERS original data copyright United States Government. No endorsement implied. Last modified 6/6/2012

Warning: the drugs or drug combinations referred to here may be similar or related, but are not be the same ones and may not have the same pharmacological action as other substances described on the same page or in the same row. Please refer to product monograph or to your doctor
This website is accredited by Health On the Net Foundation. Click to verify.
We comply with the HONcode standard for trustworthy health information: verify here.
About Reference.MD Privacy