| BPAG | bullous pemphigoid antigen |
|---|---|
| CBDC | chronic bullous disease of children |
| DEB | diepoxybutane; diethylbutanediol; Division of Environmental Biology; dystrophic epidermolysis bullos... |
| DEBRA | Dystrophic Epidermolysis Bulosa Research Association |
| DEBS | dominant epidermolysis bullosa simplex |
| bullous oedema | A reddened, swollen appearance of the ureteral orifice in the bladder wall, frequently observed with distal ureteral calculi or in tuberculosis of the ureter. (05 Mar 2000) |
|---|---|
| bullous oedema vesicae | A prominent area of focal oedema involving the bladder mucosa, consisting of elevated masses of edematous tissue or clusters of clear fluid-filled vesicles; often associated with chronic inflammation or irritation secondary to tubes, foreign bodies, or perivesical inflammation. (05 Mar 2000) |
| bullous pemphigoid | <dermatology> Form of pemphigoid (which also affects mucous membranes), in which blisters (bulli) form on the skin. Patients have circulating antibody (usually IgG) to basement membrane of stratified epithelium although the antibody titre does not correlate with the severity of the disease. (18 Nov 1997) |
| bullous pemphiguoid | A disease characterised by tense blistering eruptions of the skin. Caused by antibodies abnormally accumulating in a layer of the skin called the basement membrane. Can be chronic and mild without affecting the general health. It is diagnosed by skin biopsy showing the abnormal antibodies deposited in the skin layer. Treatment is with topical cortisone creams, but sometimes requires high doses of cortisone ( steroids ) taken internally. (12 Dec 1998) |
| bullous syphilid | A rare manifestation of congenital syphilis. Synonym: pemphigoid syphilid. (05 Mar 2000) |
| pemphigoid, bullous | A chronic and relatively benign subepidermal blistering disease usually of the elderly and without histopathologic acantholysis. (12 Dec 1998) |
| chronic bullous dermatosis of childhood | A rare self-limiting bullous disease, chiefly of the trunk, perioral, and pelvic areas, with onset in the first decade, successively less severe recurrences, and total remission at adolescence; linear epidermal basement membrane zone deposit of IgA is found in involved and in normal skin. Synonym: linear IgA bullous disease in children. (05 Mar 2000) |
| dermolytic bullous dermatosis | 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) |
| linear IgA bullous disease in children | A rare self-limiting bullous disease, chiefly of the trunk, perioral, and pelvic areas, with onset in the first decade, successively less severe recurrences, and total remission at adolescence; linear epidermal basement membrane zone deposit of IgA is found in involved and in normal skin. Synonym: linear IgA bullous disease in children. (05 Mar 2000) |
| Albright's hereditary osteodystrophy | An inherited form of hyperparathyroidism associated with ectopic calcification and ossification and skeletal defects, notably the small fourth metacarpals, but intelligence is normal. There are dominant, recessive and X-linked forms. See: pseudohypoparathyroidism. Synonym: Albright's syndrome. (05 Mar 2000) |
| angioedema, hereditary | A genetic form of angioedema. (Angioedema is also referred to as Quinke's disease.) Persons with it are born lacking an inhibitor protein (called C1 esterase inhibitor) that normally prevents activation of a cascade of proteins leading to the swelling of angioedema. Patients can develop recurrent attacks of swollen tissues, pain in the abdomen, and swelling of the voice box (larynx) which can compromise breathing. The diagnosis is suspected with a history of recurrent angioedema. It is confirmed by finding abnormally low levels of C1 esterase inhibitor in the blood. Treatment options include antihistamines and male steroids (androgens) that can also prevent the recurrent attacks. Also called hereditary angioneurotic oedema. (12 Dec 1998) |
| angioneurotic oedema, hereditary | A genetic form of angioedema. (Angioedema is also referred to as Quinke's disease.) Persons with it are born lacking an inhibitor protein (called C1 esterase inhibitor) that normally prevents activation of a cascade of proteins leading to the swelling of angioedema. Patients can develop recurrent attacks of swollen tissues, pain in the abdomen, and swelling of the voice box (larynx) which can compromise breathing. The diagnosis is suspected with a history of recurrent angioedema. It is confirmed by finding abnormally low levels of C1 esterase inhibitor in the blood. Treatment options include antihistamines and male steroids (androgens) that can also prevent the recurrent attacks. Also called hereditary angioedema. (12 Dec 1998) |
| canine hereditary blindness | An autosomal dominant condition seen in dogs of the collie and several other breeds. (05 Mar 2000) |
| colourectal neoplasms, hereditary nonpolyposis | A syndrome characterised by autosomal dominant inheritance, a low mean age (41 years) for occurrence of colon cancer, and a marked increase in the proportion of tumours in the proximal colon. (12 Dec 1998) |
| corneal dystrophies, hereditary | Bilateral hereditary disorders of the cornea, usually autosomal dominant, which may be present at birth but more frequently develop during adolescence and progress slowly throughout life. Central macular dystrophy is transmitted as an autosomal recessive defect. (12 Dec 1998) |