| CDP | chondrodysplasia punctata; chronic destructive periodontitis; collagenase-digestible protein; contin... |
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| CDPR | chondrodysplasia punctata, rhizomelic |
| CDPX | X-linked chondrodysplasia punctata |
| CP | candle power; capillary pressure; cardiac pacing; cardiac performance; cardiopulmonary; caudate puta... |
| CPXD | chondrodysplasia punctata, X-linked dominant |
| inverted follicular keratosis | A solitary benign epithelial tumour of infundibular hair follicle origin occurring on the face, consisting of a lobulated epidermal downgrowth of keratinizing squamous cells with a pattern of eddies or whorls. (05 Mar 2000) |
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| tar keratosis | Warty lesions of the face and hands resulting from repeated, prolonged exposure to tar and pitch; also occurs as keratoacanthoma-like lesions that can become malignant, particularly on the scrotum. (05 Mar 2000) |
| keratosis | <dermatology> A skin lesion that is abnormally sensitive to the effects of ultraviolet light (sunlight). Thought to be a precancerous skin lesion that is more common in the fair-skinned or elderly individual. Approximately 20% of these skin lesions will develop into squamous cell carcinoma. Prevention includes the use of sun screen agents and the avoidance of drugs (for example tetracyclines) known to cause photosensitivity reactions. Usually a discreet slightly raised, red or pink lesion located on a sun exposed surface. Texture may appear as rough, gritty or scaly. Growths may be biopsied to look for cancer or removed via cryotherapy or electrical cautery. Some topical agents may be used to promote peeling. (27 Sep 1997) |
| keratosis blennorrhagica | Pustules and crusts associated with Reiter's syndrome. Synonym: keratoderma blennorrhagica. (05 Mar 2000) |
| keratosis diffusa foetalis | most common form of ichthyosis characterised by prominent scaling especially on the exterior surfaces of the extremities. It is inherited as an autosomal dominant trait. (12 Dec 1998) |
| keratosis follicularis | A slowly progressive autosomal dominant disorder of keratinization characterised by pinkish-to-tan papules that coalesce to form plaques. These lesions become darker over time and commonly fuse, forming papillomatous and warty malodorous growths. (12 Dec 1998) |
| keratosis follicularis contagiosa | A rare condition simulating keratosis follicularis. Synonym: Brooke's disease. (05 Mar 2000) |
| keratosis labialis | Thickening of stratum corneum on the lips. (05 Mar 2000) |
| keratosis nigricans | <radiology> Pre-malignant skin disorder, papillomatosis, pigmentation, hyperkeratosis, multiple filling defects in oesophagus, increased risk of carcinoma in stomach and abdomen (12 Dec 1998) |
| keratosis obturans | An accretion of epithelia in the external auditory canal. Synonym: laminated epithelial plug. (05 Mar 2000) |
| keratosis palmaris et plantaris | The occurrence of symmetrical diffuse or patchy areas of hypertrophy of the horny layer of the epidermis on the palms and soles; a group of ectodermal dysplasias of considerable variety, and either autosomal dominant or recessive inheritance. Synonym: ichthyosis palmaris et plantaris, keratoderma palmaris et plantaris, keratoderma symmetrica, keratoma plantare sulcatum, keratosis palmaris et plantaris, tylosis palmaris et plantaris. (05 Mar 2000) |
| keratosis pilaris atrophicans faciei | Erythema and horny plugs of outer portions of the eyebrows with destruction of follicles; onset in early infancy. (05 Mar 2000) |
| keratosis rubra figurata | A dermatosis characterised by hyperkeratotic plaques of bizarre, geographic configuration, associated with erythrodermic areas that may vary remarkably in size, shape, and position from day to day; onset is usually in the first year of life; autosomal dominant inheritance. Synonym: keratosis rubra figurata. (05 Mar 2000) |
| keratosis, seborrheic | Benign eccrine poromas that present as multiple oval, brown-to-black plaques, located mostly on the chest and back. The age of onset is usually in the fourth or fifth decade. (12 Dec 1998) |
| keratosis vegetans | A slowly progressive autosomal dominant disorder of keratinization characterised by pinkish-to-tan papules that coalesce to form plaques. These lesions become darker over time and commonly fuse, forming papillomatous and warty malodorous growths. (12 Dec 1998) |