| EBA | epidermolysis bullosa acquisita; epidermolysis bullosa atrophicans; orthoethoxybenzoic acid |
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| DEB | diepoxybutane; diethylbutanediol; Division of Environmental Biology; dystrophic epidermolysis bullos... |
| DEBS | dominant epidermolysis bullosa simplex |
| EB | elective abortion; electron beam; elementary body; emotional behavior; endometrial biopsy; epidermol... |
| EBD | epidermolysis bullosa dystrophica |
| DEB | Dystrophic Epidermolysis Bullosa |
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| EB | Epidermolysis Bullosa |
| EBS | Epidermolysis Bullosa Simplex |
| EBA | Epidermolysis bullosa acquisita |
| GABEB | Generalised atrophic benign epidermolysis bullosa |
| epidermolysis bullosa | This represents a group of rare inherited disorders in which blistering of the skin occurs in response to skin trauma. Large fluid-filled blisters can occur in response to injury, skin rubbing, chafing or even increases in room temperature. Secondary bacterial infection of the blisters is common. Complications include oesophageal stricture, infections, loss of function of hands and feet and malnutrition. The dermatologist is the expert in the evaluation and treatment of this disorder. (27 Sep 1997) |
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| epidermolysis bullosa acquisita | Form of epidermolysis bullosa characterised by trauma-induced, subepidermal blistering with no family history of the disease. Direct immunofluorescence shows IgG deposited at the dermo-epidermal junction. (12 Dec 1998) |
| epidermolysis bullosa dystrophica | Form of epidermolysis bullosa characterised by atrophy of blistered areas, severe scarring, and nail changes. It is most often present at birth or in early infancy and occurs in both autosomal dominant and recessive forms. (12 Dec 1998) |
| epidermolysis bullosa, junctional | Form of epidermolysis bullosa having onset at birth or during the neonatal period and transmitted through autosomal recessive inheritance. It is characterised by generalised blister formation, extensive denudation, and separation and cleavage of the basal cell plasma membranes from the basement membrane. (12 Dec 1998) |
| epidermolysis bullosa lethalis | Epidermolysis bullosa in which the bullae are persistent, nonhealing, and often present in the oral mucosa and trachea, but not on the palms and soles, leading to death. Synonym: epidermolysis bullosa, junctional type, Herlitz syndrome. (05 Mar 2000) |
| epidermolysis bullosa simplex | This represents a group of rare inherited disorders in which blistering of the skin occurs in response to skin trauma. Large fluid-filled blisters can occur in response to injury, skin rubbing, chafing or even increases in room temperature. Secondary bacterial infection of the blisters is common. Complications include oesophageal stricture, infections, loss of function of hands and feet and malnutrition. The dermatologist is the expert in the evaluation and treatment of this disorder. (27 Sep 1997) |
| acrodermatitis chronica atrophicans | A gradually progressive late skin manifestation of Lyme disease, appearing first on the feet, hands, elbows or knees, and comprised of indurated, erythematous plaques that become atrophic, giving a tissue-paper appearance of the involved sites. The disease is caused by Borrelia spirochetes, commonly transmitted by the Ixodes ricinus wood tick. (05 Mar 2000) |
| poikiloderma atrophicans and cataract | The rothmund-thomson syndrome, a genetic disorder with numerous features affecting skin (premature aging, excess pigmentation, dilated blood vessels),eyes ( uvenile cataract), nose (saddle nose), teeth (maldeveloped), skeletal system (congenital bone defects) hair (abnormal), gonads (underdevelopment) limbs (soft tissue contractures), growth (short stature). Blood (anaemia) and a tendency to develop a type of bone cancer (osteogenic sarcoma). The rts gene is on chromosome 8. The syndrome is recessive so to be affected with rts a child has to have two rts genes, one from each parent. (12 Dec 1998) |
| poikiloderma atrophicans vasculare | A rare condition that simulates chronic radiodermatitis in appearance; may eventuate as mycosis fungoides. Synonym: parakeratosis variegata, parapsoriasis lichenoides. Poikiloderma of Civatte, reticulated pigmentation and telangiectasia of the sides of the cheeks and neck; common in middle-aged women. Synonym: Civatte's disease. (05 Mar 2000) |
| dermatitis atrophicans | A diffuse idiopathic atrophy of the skin involving the appendages. (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) |
| lichen planus et acuminatus atrophicans | Follicular hyperkeratosis of the scalp with lymphocytic perifolliculitis and lichen planus elsewhere. Synonym: Graham Little syndrome, lichen planus et acuminatus atrophicans. (05 Mar 2000) |
| epidermolysis | A condition in which the epidermis is loosely attached to the corium, readily exfoliating or forming blisters. Origin: epidermis + G. Lysis, loosening (05 Mar 2000) |
| concha bullosa | Abnormal pneumatization of the middle turbinate which may interfere with normal ventilation of sinus ostia and can result in recurrent sinusitis. (05 Mar 2000) |
| Pseudostertagia bullosa | One of the medium stomach worms located in the abomasum of sheep, goats, and pronghorn; it is found chiefly in the western U.S. (05 Mar 2000) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|