| DVIS | digital vascular imaging system |
|---|---|
| PNS | Peripheral Nervous System; |
| PAS | para aminosalicylate; Parent Attitude Scale; patient administration system; patient appointments and... |
| CNS | central nervous system; clinical nurse specialist; coagulase-negative staphylococci; congenital neph... |
| CRS | Carroll rating scale for depression; catheter-related sepsis; caudal regression syndrome; cervical s... |
| mesenteric vascular occlusion | Obstruction of the flow in the mesenteric circulation by atherosclerosis, emboli or thrombi, stenosis, trauma, and compression or intrinsic pressure from adjacent tumours. Rare causes are drugs, intestinal parasites, and vascular immunoinflammatory diseases such as periarteritis nodosa and thromboangiitis obliterans. (12 Dec 1998) |
|---|---|
| choroidal vascular atrophy | Atrophy affecting either all choroidal vessels or only the choriocapillaris, occurring either diffusely or confined to the posterior pole of the eye. (05 Mar 2000) |
| collagen-vascular diseases | A group of generalised disease's affecting connective tissue and frequently characterised by fibrinoid necrosis or vasculitis; in some collagen disease's, auto-immunization, particularly antinuclear antibodies, has been shown and circulating immune complexes are found. The term is not entirely acceptable because there is no evidence that collagen is primarily involved; "collagen" was once synonymous with "connective tissue" rather than describing a specific fibrinous protein in that tissue. See: connective-tissue diseases. (05 Mar 2000) |
| muscle, smooth, vascular | The nonstriated, involuntary muscle tissue of blood vessels. (12 Dec 1998) |
| Haller's vascular tissue | <anatomy> The outer portion of the choroid of the eye containing the largest blood vessels. Synonym: lamina vasculosa choroideae, Haller's vascular tissue, uvaeformis, vascular layer of choroid coat of eye, vascular layer. (05 Mar 2000) |
| skin diseases, vascular | Skin diseases affecting or involving the cutaneous blood vessels and generally manifested as inflammation, swelling, erythema, or necrosis in the affected area. (12 Dec 1998) |
| neoplasms, vascular tissue | Neoplasms composed of vascular tissue. This concept does not refer to neoplasms located in blood vessels. (12 Dec 1998) |
| dementia, vascular | An organic mental disorder caused by systemic vascular disease such as arteriosclerotic changes in the vessels, valvular heart disease, hypertension, etc., and resulting in cerebral vascular disease with dementia. (12 Dec 1998) |
| systemic vascular resistance | An index of arteriolar compliance or constriction throughout the body; equal to the blood pressure divided by the cardiac output. (05 Mar 2000) |
| encephalotrigeminal vascular syndrome | <syndrome> Angiomatosis of the brain accompanied by nevi in the trigeminal area. See: Sturge-Weber syndrome. (05 Mar 2000) |
| endothelium, vascular | Single pavement layer of cells which line the luminal surface of the entire vascular system and regulate the transport of macromolecules and blood components from interstitium to lumen; this function has been most intensively studied in the blood capillaries. (12 Dec 1998) |
| Zinn's vascular circle | <anatomy, nerve> A network of branches of the short ciliary arteries on the sclera around the point of entrance of the optic nerve. Synonym: circulus vasculosus nervi optici, circulus arteriosus halleri, circulus zinnii, Haller's circle, Zinn's corona, Zinn's vascular circle. (05 Mar 2000) |
| adrenal hyperplasia, congenital | A group of inherited disorders of adrenal steroidogenesis, the physical expression of which varies with the sex of the patient, the severity of the congenital enzyme defect, and the age at which the defect makes its presence felt. The most common form, the simple virilizing form, is due to a 21-hydroxylase deficiency. There is also a salt-losing form (a more complete 21-hydroxylase deficiency), a hypertensive form (11-hydroxylase deficiency), a 17-hydroxylase deficiency form, a desmolase deficiency form, and a 3-beta-hydroxysteroid deficiency form. (12 Dec 1998) |
| anaemia, dyserythropoietic, congenital | A familial disorder characterised by anaemia with multinuclear erythroblasts, karyorrhexis, asynchrony of nuclear and cytoplasmic maturation, and various nuclear abnormalities of bone marrow erythrocyte precursors. Type II is the most common of the 3 types of congenital dyserythropoietic anaemia; it is often referred to as hempas, based on the hereditary erythroblast multinuclearity with positive acidified serum test. (12 Dec 1998) |
| anaemia, haemolytic, congenital | Haemolytic anaemia due to various intrinsic defects of the erythrocyte. (12 Dec 1998) |