| CPC | central posterior curve; cerebellar Purkinje cell; cerebral palsy clinic; cerebral performance categ... |
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| CPOTHA | chest pain onset to hospital arrival |
| CPP | cancer proneness phenotype; canine pancreatic polypeptide; cerebral perfusion pressure; chest pain p... |
| CPSP | central poststroke pain |
| CPUE | chest pain of unknown etiology |
| budding and appendaged bacteria | Bacteria that commonly possess unusual shapes, have complex life cycles, and divide by budding. Many have appendages which are sufficiently prominent that they can be detected by phase-contrast light microscopy. (12 Dec 1998) |
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| Burn and Rand theory | That stimulation of sympathetic fibres results first in the production of acetylcholine in the postganglionic nerve endings, which then release norepinephrine to act on the active site of the effector cell. (05 Mar 2000) |
| caffeine and sodium benzoate | A mixture of equal parts of sodium benzoate and caffeine, used to meet the indication of caffeine. (05 Mar 2000) |
| caffeine and sodium salicylate | A mixture of sodium salicylate and caffeine used for the relief of headache and neuralgia. (05 Mar 2000) |
| calcifying and keratinizing odontogenic cyst | A mixed radiolucent-radiopaque lesion of the jaws with features of both a cyst and a solid neoplasm; characterised microscopically by an epithelial lining showing a palisaded layer of columnar basal cells, presence of ghost cell keratinization, dentinoid, and calcification. Synonym: calcifying and keratinizing odontogenic cyst, Gorlin cyst. (05 Mar 2000) |
| cancer, colon: screening and surveillance | Colon cancer is both preventable and curable. It is preventable by removing precancerous colon polyps. It is curable if early cancer is surgically removed before cancer spread to other parts of the body. Therefore, if screening and surveillance programs were practiced universally, there would be a major reduction in the incidence and mortality of colon cancer. (12 Dec 1998) |
| carbohydrates and hypoglycaemic agents | A collective term for carbohydrates and agents used to lower the level of glucose in the blood. (12 Dec 1998) |
| carboxyl and carbamoyl transferases | <enzyme> A group of enzymes that catalyze the transfer of carboxyl- or carbamoyl- groups. Registry number: EC 2.1.3 (12 Dec 1998) |
| Gaddum and Schild test | A sensitive method for identification of epinephrine in tissue or other material, based on the fluorescence of epinephrine exposed to ultraviolet light in the presence of alkali and oxygen; sensitivity ranges from 1:50 to 1:100 million. (05 Mar 2000) |
| vaginal creams, foams and jellies | Medicated dosage forms for topical application in the vagina. A cream is a semisolid emulsion containing suspended or dissolved medication; a foam is a dispersion of a gas in a medicated liquid resulting in a light, frothy mass; a jelly is a colloidal semisolid mass of a water soluble medicated material, usually translucent. The concept includes vaginal creams, foams, and jellies in general or for which there is no other specific heading. (12 Dec 1998) |
| magnesia and alumina oral suspension | A mixture of magnesium hydroxide and variable amounts of aluminum oxide; used as an antacid. (05 Mar 2000) |
| maintenance and engineering, hospital | Hospital department whose primary function is the upkeep and supervision of the buildings and grounds and the maintenance of hospital physical plant and equipment which requires engineering expertise. (12 Dec 1998) |
| P and P test | A test formerly used by some to control anticoagulant therapy with bishydroxycoumarin and indandione drugs. Synonym: P and P test. (05 Mar 2000) |
| malignancy and immunodeficiency | <radiology> High risk of malignancy (especially lymphoma/leukaemia, GI tumours): X-linked agammaglobulinaemia (Bruton's), common variable immunodeficiency, severe combined immunodeficiency (SCID kids), ataxia-telangectasia, Wiscott-Aldrich syndrome, selective IgA deficiency (12 Dec 1998) |
| Papillon-Leage and Psaume syndrome | <syndrome> An inherited syndrome, lethal in males, with varying combinations of defects of the oral cavity, face, and hands, including lobulated or bifid tongue, cleft or pseudocleft palate, tongue tumours, missing or malpositioned teeth, hypoplastic nasal alar cartilage, depressed nasal bridge, brachydactyly, clinodactyly, incomplete syndactyly, and, frequently, mental retardation. There are two subtypes recognised. Type I (papillon-leage and psaume syndrome, gorlin-psaume syndrome) is inherited as an x-linked dominant trait and is found only in females and XXY males. Type II (mohr syndrome) is inherited as an autosomal recessive trait. Inheritance: autosomal recessive and X-linked. Synonym: OFD syndrome, orofaciodigital syndrome, Papillon-Leage and Psaume syndrome. (05 Mar 2000) |