| DC | daily census; data communication; data conversion; decrease; deep compartment; Dental Corps; deoxych... |
|---|---|
| DKC | dyskeratosis congenita |
| IFAP | ichthyosis follicularis-atrichia-photophobia [syndrome] |
| KFSD | keratosis follicularis spinulosa decalvans |
| KFSD | Keratosis follicularis spinulosa decalvans |
|---|---|
| DC | Dyskeratosis Congenita |
| DKC | Dyskeratosis congenita |
| isolated dyskeratosis follicularis | warty dyskeratoma |
|---|---|
| benign dyskeratosis | Dyskeratosis that may occur in congenital and bullous diseases of the skin. (05 Mar 2000) |
| malignant dyskeratosis | Dyskeratosis that may occur in precancerous or malignant lesions. (05 Mar 2000) |
| hereditary benign intraepithelial dyskeratosis | An autosomal dominant condition consisting of white spongy lesions of the buccal mucosa, floor of the mouth, ventral lateral tongue, gingiva and palate. Transient gelatinous plaques form over the cornea, which may produce temporary blindness, hereditary benign intraepithelial dyskeratosis. Synonym: hereditary benign intraepithelial dyskeratosis. (05 Mar 2000) |
| dyskeratosis | 1. Premature keratinization of epithelial cells that have not reached the keratinizing surface layer; dyskeratotic cells generally become rounded and they may break away from adjacent cells and fall off. 2. Epidermalization of the conjunctival and corneal epithelium. 3. A disorder of keratinization. Origin: dys-+ G. Keras, horn, + -osis, condition (05 Mar 2000) |
| dyskeratosis congenita | An x-linked syndrome occurring predominantly in males, with onset in childhood and characterised by nail dystrophy, reticular cutaneous hyperpigmentation, mucosal leukokeratosis, and pancytopenia resembling that of fanconi. It is also known as zinsser-cole-engman syndrome. (12 Dec 1998) |
| intraepithelial dyskeratosis | An autosomal dominant condition consisting of white spongy lesions of the buccal mucosa, floor of the mouth, ventral lateral tongue, gingiva and palate. Transient gelatinous plaques form over the cornea, which may produce temporary blindness, hereditary benign intraepithelial dyskeratosis. Synonym: hereditary benign intraepithelial dyskeratosis. (05 Mar 2000) |
| hyperkeratosis follicularis et parafollicularis | Discrete and confluent horny follicular plugs on a crateriform base, often occurring on the arms and legs in diabetics with renal failure; possibly a severe form of perforating folliculitis. Synonym: hyperkeratosis penetrans, Kyrle's disease. (05 Mar 2000) |
| nevus follicularis keratosis | Comedo nevus, congenital or childhood linear keratinous cystic invaginations of the epidermis, with failure of development of normal pilosebaceous follicles. Synonym: nevus follicularis keratosis. (05 Mar 2000) |
| ichthyosis follicularis | A form of autosomal dominant type of ichthyosis, with horny follicular plugging of the extensor surfaces of the extremities; onset in early childhood. (05 Mar 2000) |
| tuberculosis cutis follicularis disseminata | Dusky-red papules followed by crusting and ulceration primarily on the extremities and predominantly in young adults with a deep focus of tuberculosis or with a history of preceding infection. Synonym: tuberculosis cutis follicularis disseminata, tuberculosis papulonecrotica. (05 Mar 2000) |
| 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) |
| lichen planus follicularis | Lichen planus of the hair follicles, usually of the scalp. (05 Mar 2000) |
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