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| ¿µ¹® | mast cell | ÇÑ±Û | ºñ¸¸ ¼¼Æ÷ |
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| CD | cadaver donor; canine distemper; canine dose; carbohydrate dehydratase; carbon dioxide; cardiac dise... |
|---|---|
| HD | Haab-Dimmer [syndrome]; Hajna-Damon [broth]; Hansen disease; hearing distance; heart disease; helix ... |
| MD | Doctor of Medicine [Lat. Medicinae Doctor]; magnesium deficiency; main duct; maintenance dose; major... |
| ID | identification; iditol dehydrogenase; immunodeficiency; immunodiffusion; immunoglobulin deficiency; ... |
| AD | accident dispensary; acetate dialysis; active disease; acute dermatomyositis; addict, addiction; ade... |
| GPIC | Guinea pig inclusion conjunctivitis |
|---|---|
| IBH | Inclusion Body Hepatitis |
| IB | Inclusion bodies |
| IBM | Inclusion body myositis |
| LBHI | Lewy body-like hyaline inclusion |
Kugelberg-Welander disease ±Ù À§ÃàÁõÀÇ À¯Àü¼º ¿¬¼ÒÇüÀ¸·Î¼ º¸Åë »ó¿°»öü¼º ¿¼º ÇüÁú·Î À¯ÀüµÈ´Ù. ô¼ö Àü°¢ÀÇ º´º¯ÀÌ ±× ¿øÀÎÀÌ´Ù.
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| inclusion cell disease | <biochemistry> Mucolipidosis of early onset and with severe symptoms like those in Hurler's syndrome but with normal urinary mucopolysaccharides, vacuolated lymphocytes, and inclusion bodies in cultured fibroblasts (I-cells). The lysosomes lack hydrolases but high concentrations of lysosomal enzymes are found in the extracellular fluids such as serum, spinal fluid, and urine. It is associated with a deficiency of N-acetylglucosaminyl-1-phosphotransferase. The gene defect responsible probably prevents the addition of the lysosome recognition marker mannose 6 phosphate) to these enzymes so that they are not directed into the lysosomes but are released. Inheritance: autosomal recessive. Synonym: I-cell disease, inclusion cell disease. (12 Jul 2000) |
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| inclusion cell | i cell |
|---|---|
| cytomegalic inclusion 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 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) |
| 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) |
| conjunctivitis, inclusion | An infection of the eyes characterised by the presence in conjunctival epithelial cells of inclusion bodies indistinguishable from those of trachoma. It is acquired by infants during birth and by adults from swimming pools. The aetiological agent is chlamydia trachomatis whose natural habitat appears to be the genito-urinary tract. Inclusion conjunctivitis is a less severe disease than trachoma and usually clears up spontaneously. (12 Dec 1998) |
| Cowdry's type A inclusion bodies | Droplet-like masses of acidophilic material surrounded by clear halos within nuclei, with margination of chromatin on the nuclear membrane. (05 Mar 2000) |
| Cowdry's type B inclusion bodies | Droplet-like masses of acidophilic material surrounded by clear halos within nuclei, without other nuclear changes during early stages of development of the inclusion. (05 Mar 2000) |
| 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) |
| cytoplasmic inclusion bodies | See: inclusion bodies. (05 Mar 2000) |
| psittacosis inclusion bodies | Intracytoplasmic chlamydial microcolonies observed in bronchial epithelial cells infected with Chlamydia psittaci. (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) |
| nuclear inclusion bodies | See: inclusion bodies. (05 Mar 2000) |
| inclusion | 1. The act of including, or the state of being included; limitation; restriction; as, the lines of inclusion of his policy. 2. <chemical> A foreign substance, either liquid or solid, usually of minute size, inclosed in the mass of a mineral. Origin: L. Inclusio: cf. F. Inclusion. See Include. Source: Websters Dictionary (01 Mar 1998) |
| inclusion blennorrhoea | A neonatal conjunctivitis caused by Chlamydia trachomatis. (05 Mar 2000) |
| inclusion bodies | <cell biology> Nuclear or cytoplasmic structures with characteristic staining properties, usually found at the site of virus multiplication. Semi crystalline arrays of virions, capsids or other viral components. (13 Nov 1997) |
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