| CIBHA | congenital inclusion-body hemolytic anemia |
|---|---|
| IBM | inclusion body myositis |
| IncB | inclusion body |
| LB | lamellar body; large bowel; left breast; left bronchus; left bundle; left buttock; leiomyoblastoma; ... |
| TBS | total body solids; total body solute; total body surface; total burn size; Townes-Brocks syndrome; t... |
| 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) |
| inclusion bodies, viral | An area showing altered staining behaviour in the nucleus or cytoplasm of a virus-infected cell. Some inclusion bodies represent "virus factories" in which viral nucleic acid or protein is being synthesised; others are merely artifacts of fixation and staining. One example, negri bodies, are found in the cytoplasm or processes of nerve cells in animals that have died from rabies. (12 Dec 1998) |
| inclusion cell | i cell |
| 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) |
| inclusion compound | The mechanical trapping of small molecules within spaces between other molecules; e.g., the inclusion of iodine molecules by starch molecules to form the well-known red-to-black "addition compound" (05 Mar 2000) |
| inclusion conjunctivitis | A follicular conjunctivitis caused by Chlamydia trachomatis. (05 Mar 2000) |
| inclusion conjunctivitis viruses | Former name for Chlamydia trachomatis. (05 Mar 2000) |
| inclusion cyst | Intradermal or subcutaneous saclike structure, the wall of which is stratified epithelium containing keratohyalin granules. (12 Dec 1998) |
| inclusion dermoid | A collection of cancerous cells which form cysts that contain one or more of the three primary embryonic germ layers: skin, hair or teeth. (27 Sep 1997) |
| epidermoid inclusion cyst | <radiology> Well-circumscribed radiolucent lesion showing a thin cortical margin that may not be visible in its entirety, frequently in the terminal phalanx, history of penetrating trauma is often elicited Differential diagnosis: ABC, enchondroma (12 Dec 1998) |
| foetal inclusion | Unequal conjoined twins in which the incompletely developed parasite is wholly enclosed in the autosite. (05 Mar 2000) |
| acetone body | <biochemistry> Any of the three compounds created by acetyl coenzyme A (acetoacetate, hydroxybutyrate, and acetone) which are water-soluble cellular fuels normally exported by the liver. They can build up in the blood and body tissues because of starvation, untreated diabetes mellitus, or other disorders that interfere with carbohydrate metabolism. The body rids itself of ketones mainly through urine, but it rids itself of acetone through the lungs, which gives the breath a characteristic fruity odour. If ketones build up in the body long enough, they cause serious illness and coma (see ketoacidosis.) (09 Oct 1997) |