| IBB | intestinal brush border |
|---|---|
| IGP | intestinal glycoprotein |
| IIP | idiopathic interstitial pneumonia; idiopathic intestinal pseudo-obstruction; increased intracranial ... |
| IMC | indigent medical care; information-memory-concentration [test]; interdigestive migrating contraction... |
| INT | intermediate; intermittent; intern, internship; internal; interval; intestinal; intima; p-iodonitrot... |
| intestinal pseudo-obstruction | <radiology> Chronic idiopathic intestinal pseudo-obstruction, autosomal dominant, variable penetrance, insidious onset in child or young adult, intermittent episodes, dysphagia, vomiting, abdominal pain/distention, diarrhoea, constipationn, small bowel involvement most common, megaduodenum, ileus simulating obstruction (12 Dec 1998) |
|---|---|
| intestinal rotation | See: malrotation. Molecular rotation, one hundredth of the product of the specific rotation of an optically active compound and its molecular weight. Optical rotation, the change in the plane of polarization of polarised light of a given wavelength upon passing through optically active substances; measured in terms of specific rotation by polarimetry, an important tool in chemical structural work, especially on carbohydrates. Specific optical rotation ([a]), the arc through which the plane of polarised light is rotated by 1 gram of a substance per milliliter of water when the length of the light path through the solution is 1 decimeter, typically using light corresponding to the D line of sodium. (05 Mar 2000) |
| intestinal sand | Minute calculi or gritty material occurring in faeces, composed of soaps, bile pigment, cholesterol, magnesium salts, succinic acid, etc. (05 Mar 2000) |
| intestinal schistosomiasis | Schistosomiasis caused by schistosoma mansoni. It is endemic in africa, the middle east, south america, and the caribbean and affects mainly the bowel, spleen, and liver. (12 Dec 1998) |
| intestinal stasis | Intestinal stasis; a retardation or arrest of the passage of the intestinal contents. Synonym: intestinal stasis. Origin: entero-+ G. Stasis, a standing (05 Mar 2000) |
| intestinal steatorrhoea | Steatorrhoea due to malabsorption resulting from intestinal disease. See: sprue, coeliac disease. (05 Mar 2000) |
| intestinal surface of uterus | The posterosuperior surface of the uterus with which loops of intestine come in contact. Synonym: facies intestinalis uteri. (05 Mar 2000) |
| intestinal tract | <anatomy> This includes the coarse of the small and large intestines and includes approximately 27 feet of bowel. (27 Sep 1997) |
| intestinal villi | <pathology> Microscopic finger-like projections (0.5 to 1.5 mm in length) off of the mucosal lining of the small intestine which are responsible for absorption of nutrients. The villi greatly increase the effective absorptive surface area of the small intestine. (27 Sep 1997) |
| juxta-intestinal lymph nodes | The mesenteric lymph nodes located in immediate proximity to the jejunum or ileum. Synonym: nodi lymphatici juxta-intestinales. (05 Mar 2000) |
| familial intestinal polyposis | Begins usually in late childhood; polyps increase in numbers, causing symptoms of chronic colitis, and carcinoma of the colon almost invariably develops in untreated cases; autosomal dominant inheritance. In the Gardner syndrome there are extracolonic changes (desmoid tumours, etc.). Synonym: polyposis coli. Hamartomatous polyposis of the small or large intestine, Peutz-Jeghers syndrome with melanin spots on the lips, less common, miscellaneous, rare, and doubtful occurrences. Synonym: familial intestinal polyposis. (05 Mar 2000) |
| lieno-intestinal | <anatomy> Of or pertaining to the spleen and intestine; as, the lieno-intestinal vein of the frog. Origin: l. Lien the spleen + E. Intestinal. Source: Websters Dictionary (01 Mar 1998) |
| lipophagic intestinal granulomatosis | An obsolete term for Whipple's disease. (05 Mar 2000) |
| lymphangiectasis, intestinal | Dilatation of the intestinal lymphatic system, particularly in the lacteals in the intestinal villi, characterised by protein-losing enteropathy, steatorrhoea, and lymphopenia. It may be congenital, due to abnormality of the lymphatic system (as in milroy's disease) or acquired, due to involvement of the major intestinal lymphatic ducts by inflammatory processes or neoplasm, or to increased lymphatic pressure, as in valvular heart disease and constrictive pericarditis. (12 Dec 1998) |