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| IBM | inclusion body myositis |
|---|---|
| IB | idiopathic blepharospasm; immune body; inclusion body; index of body build; infectious bronchitis; I... |
| DM | 1) Diabetes Mellitus 2) Dermato-Myositis |
| AIE | acute inclusion-body encephalitis; acute infectious encephalitis; acute infective endocarditis |
| CIBHA | congenital inclusion-body hemolytic anemia |
| IBM | Inclusion body myositis |
|---|---|
| S-IBM | Sporadic inclusion body myositis |
| IBH | Inclusion Body Hepatitis |
| LBHI | Lewy body-like hyaline inclusion |
| GPIC | Guinea pig inclusion conjunctivitis |
| inclusion body myositis | <radiology> Common form of inflamatory myopathy, most common in the elderly, equal sex incidence, sporadic idiopathic disease (very rarely familial), misdiagnosed as steroid-resistant polymyositis symptoms, presents as a painless slowly progressive proximal myopathy, may cause dysphagia, mild to moderate muscle wasting diagnosis, serum creatine kinase levels usually normal or only slightly elevated, EMG may show non-specific myopathic features, diagnosis on muscle biopsy, inclusion bodies seen in rimmed vacuoles in skeletal muscle fibres treatment, steroids and immunosuppression generally ineffective, rare patients reported who have made a response to treatment pathogenesis, unknown, ubiquitin, prion protein, tau protein found in inclusions, abnormal mitchondria seen in some case (12 Dec 1998) |
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| myositis, inclusion body | A progressive inflammatory myopathy primarily involving muscles of the pelvic region and legs, usually seen in older people. The muscles are infiltrated by mononuclear inflammatory cells, sarcoplasmic vacuoles, masses of filaments and filamentous microtubules, and sometimes eosinophilic bodies. (12 Dec 1998) |
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| acute inclusion body encephalitis | The most common acute encephalitis, caused by HSV-1; affects persons of any age; preferentially involves the inferomedial portions of the temporal lobe and the orbital portions of the frontal lobes; pathologically, severe haemorrhagic necrosis is present along with, in the acute stages, intranuclear eosinophilic inclusion bodies in the neurons and glial cells. Synonym: acute inclusion body encephalitis, herpes encephalitis. (05 Mar 2000) |
| subacute inclusion body encephalitis | <neurology> Chronic progressive illness seen in children a few years after measles infection and involving demyelination of the cerebral cortex. Virus apparently persists in brain cells: usually considered a slow virus disease. (18 Nov 1997) |
| inclusion body disease | <disease> An illness in newborns caused by viral infection, symptoms includefever, cellular enlargement, microscopically-visible clumps of viralparticles or proteins in the cytoplasm and nuclei of affected cells, enlargementof the spleen and liver. Long-term effects of the disease may includemental retardation. (09 Oct 1997) |
| inclusion body encephalitis | <neurology> Chronic progressive illness seen in children a few years after measles infection and involving demyelination of the cerebral cortex. Virus apparently persists in brain cells: usually considered a slow virus disease. (18 Nov 1997) |
| inclusion body rhinitis | A respiratory disease of pigs caused by the cytomegalovirus porcine herpesvirus 2 and characterised by rhinitis and conjunctivitis in young pigs. (05 Mar 2000) |
| acute disseminated myositis | The occurrence of multiple foci of acute inflammation in the muscular tissue and overlying skin in various parts of the body, accompanied by fever and other signs of systemic infection. See: dermatomyositis. Synonym: acute disseminated myositis, pseudotrichinosis, pseudotrichiniasis. (05 Mar 2000) |
| cervical myositis | See: posttraumatic neck syndrome. (05 Mar 2000) |
| multiple myositis | The occurrence of multiple foci of acute inflammation in the muscular tissue and overlying skin in various parts of the body, accompanied by fever and other signs of systemic infection. See: dermatomyositis. Synonym: acute disseminated myositis, pseudotrichinosis, pseudotrichiniasis. (05 Mar 2000) |
| myositis | <pathology> Inflammation of a voluntary muscle. Origin: Gr. Myos = of muscle (18 Nov 1997) |
| myositis fibrosa | Induration of a muscle through an interstitial growth of fibrous tissue. Synonym: Froriep's induration, interstitial myositis, myofascitis. (05 Mar 2000) |
| myositis ossificans | A disease characterised by bony deposits or the ossification of muscle tissue. (12 Dec 1998) |
| myositis ossificans circumscripta | Local deposit of bone in a muscle, usually following prolonged trauma; e.g., riders' bone. (05 Mar 2000) |
| myositis ossificans progressiva | <radiology> Progressive skeletal fusion, ossification of ligaments, nuchal ligament, pelvic entheses, asymptomatic at birth, 90% have short great toes (12 Dec 1998) |
| myositis purulenta tropica | A disease observed in Samoa and in tropical Africa, marked by pains in the extremities, fever of a remittent or intermittent type, and abscesses in the muscles in various parts of the body (may result in death from sepsis); causative organisms are Staphylococcus aureus and Streptococcus pyogenes, but usually the disease is associated with parasitic infections. Synonym: bungpagga, lambo lambo, tropical myositis, tropical pyomyositis. (05 Mar 2000) |
| inclusion body myositis |
myositis characterized by weakness of limb muscles (especially the thighs and wrists and fingers); sometimes involves swallowing muscles; onset after 50 and slowly progressive; seen more often in men than in women
Ãâó: wordnet.princeton.edu/perl/webwn
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|---|---|
| inclusion body myositis |
Inclusion body myositis (IBM) is an inflammatory muscle disease characterized by slowly progressive wasting and weakness of upper extremities. Although there is profound inflammation (invasion of muscle tissue with white blood cells and related substances like antibodies and complements) in the muscle tissue just as observed in other inflammatory autoimmune disorders of the muscle (e.g. polymyositis), the cause does not seem to be autoimmunity. ...
Ãâó: en.wikipedia.org/wiki/Inclusion_body_myositis
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