| GPIMH | guinea pig intestinal mucosal homogenate |
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| HIE | human intestinal epithelium; hyper-IgE [syndrome]; hypoxic-ischemic encephalopathy |
| HIPO | hemihypertrophy, intestinal web, preauricular skin tag, and congenital corneal opacity [syndrome]; H... |
| IBB | intestinal brush border |
| IGP | intestinal glycoprotein |
| 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 trunks | The vessels conveying lymph from the lower part of the liver, the stomach, spleen, pancreas, and small intestine; they discharge into the cisterna chyli and are sometimes duplicated. Synonym: trunci intestinales. (05 Mar 2000) |
| 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) |
| anhidrotic ectodermal dysplasia | A hereditary condition (most often x linked) that is characterised by the abnormal development of skin, absence of sweat glands, dry eyes and abnormal development of teeth. Symptoms include absent teeth, peg teeth, inability to sweat, thin skin and heat intolerance. Mucous membrane involvement may result in a foul-smelling nasal discharge. The inability to sweat leads to the inability to maintain normal body temperature in a warm environment. Some may exhibit fevers and will require artificial cooling. Inheritance: mostly sex-linked (X chromosome). Origin: Gr. Plassein = to form (12 Nov 1997) |
| anterofacial dysplasia | Abnormal growth of the face or cranium in an anteroposterior direction as seen and measured with a cephalogram. (05 Mar 2000) |
| arrhythmogenic right ventricular dysplasia | A congenital cardiomyopathy in which transmural infiltration of adipose tissue results in weakness and aneurysmal bulging of the infundibulum, apex, and posterior basilar region of the right ventricle and leads to ventricular tachycardia arising in the right ventricle. (12 Dec 1998) |
| asphyxiating thoracic dysplasia | Hereditary hypoplasia of the thorax, associated with pelvic skeletal abnormality. Synonym: asphyxiating thoracic chondrodystrophy, Jeune's syndrome, thoracic-pelvic-phalangeal dystrophy. (05 Mar 2000) |
| bronchopulmonary dysplasia | <embryology, paediatrics> A form of chronic lung disease of uncertain cause sometimes seen in children who have received mechanical respiratory support (with high oxygenation) in the neonatal period. Often associated with those infants who have been treated for hyaline membrane disease. Origin: Gr. Plassein = to form (27 Sep 1997) |
| mammary dysplasia | An obsolete term for fibrocystic condition of the breast. (05 Mar 2000) |