| EBA | epidermolysis bullosa acquisita; epidermolysis bullosa atrophicans; orthoethoxybenzoic acid |
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| EBD | epidermolysis bullosa dystrophica |
| EBDCT | Cockayne-Touraine type of epidermolysis bullosa dystrophica |
| EBDD | epidermolysis bullosa dystrophica dominant |
| EBDR | epidermolysis bullosa dystrophica recessiva |
| 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 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 | 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) |
| 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, 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) |
| myotonia dystrophica | <neurology> An inherited human neuromuscular disease classed as an autosomal dominant disease in which there is progressive muscle weakening and wasting. A triplet repeat syndromes (like fragile X syndrome), this most common adult form of muscular dystrophy is caused by expansion of the unstable trinucleotide repeat CTG in the 3' untranslated region on chromosome 19q13 (cAMP-dependent muscle protein kinase gene). Anticipation has been associated with further expansion of the repeat upon transmission to subsequent generations (the inheritance pattern is autosomal dominant), although contraction has been noted to occur as well. Especially severe neonatal cases have been born to affected mothers preferentially, suggesting a role for genomic imprinting as well. The classic physical signs include atrophy of facial muscles, cataracts, and delayed muscle relaxation. Detection of the expanded trinucleotide repeat is accomplished by PCR or Southern blot and expansion appears to correlate with decreased transcription of the protein kinase gene. Inheritance: autosomal dominant. (29 Dec 1997) |
| elastosis dystrophica | Tiny breaks in the elastin-filled tissue in the back of the eye (retinae). These abnormalities are visible to the doctor during an examination using a viewing instrument called an ophthalmoscope. Angioid streaks are seen in patients with pseudoxanthoma elasticum (abbreviated PXE), a rare disorder of degeneration of the elastic fibres with tiny areas of calcification in the skin, back of the eyes (retinae), and blood vessels. Angioid streaks can be associated with blindness. (12 Dec 1998) |
| 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) |
| impetigo bullosa | Impetigo with lesions of large size, forming bullae. (05 Mar 2000) |
| impetigo contagiosa bullosa | Discrete purulent skin lesions occasionally seen with streptococcal pyoderma. (05 Mar 2000) |
| urticaria bullosa | An eruption of wheals capped with subepidermal vesicles. Synonym: urticaria vesiculosa. (05 Mar 2000) |
| persistent anterior hyperplastic primary vitreous | A unilateral congenital abnormality occurring in full-term infants; characterised by a retrolental fibrovascular membrane formed by persistent primary vitreous with remnants of the hyaloid artery and tunica vasculosa lentis; associated with leukokoria, microphthalmos, shallow anterior chamber, and elongated ciliary processes. (05 Mar 2000) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|