| FPSTS | false-positive serologic test for syphilis |
|---|---|
| HATTS | hemagglutination treponemal test for syphilis |
| LI, LII, | LIII first, second, third stage of syphilis |
| LT | heat-labile toxin; laminar tomography; left; left thigh; less than; lethal time; leukotriene; Levin ... |
| S | Greek capital letter sigma; syphilis; summation of series |
| early latent syphilis | Infection with Treponema pallidum, the organism of syphilis, after the primary and secondary phases have subsided, during the first year after infection, before any manifestations of tertiary syphilis have appeared. (05 Mar 2000) |
|---|---|
| early syphilis | Primary, secondary, or early latent syphilis, before any tertiary manifestations have appeared. (05 Mar 2000) |
| endemic syphilis | Syphilis caused by organisms closely related to Treponema pallidum; spread by personal, but not necessarily venereal, contact; usually acquired in childhood, most common in areas of provery and overcrowding; rare in the United States; includes yaws, pinta and bejel. Synonym: endemic syphilis. (05 Mar 2000) |
| equine syphilis | A disease of horses and donkeys caused by trypanosoma equiperdum. The disease occurs in africa, the americas, and asia. (12 Dec 1998) |
| late benign syphilis | Late syphilis, manifested by serologic evidence of infection, but without any clinical manifestations. (05 Mar 2000) |
| late latent syphilis | Usually infectious in pregnant women only, who may pass the infection on to the foetus. (05 Mar 2000) |
| latent syphilis | Infection with Treponema pallidum, after the manifestations of primary and secondary syphilis have subsided (or were never noticed), before any manifestations of tertiary syphilis have appeared. (05 Mar 2000) |
| late syphilis | Involvement of the cardiovascular or central nervous system, or the development of a gumma in any organ, due to infection with Treponema pallidum; usually several years to 2-3 decades after the initial infection. Synonym: tertiary syphilis. (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) |
| hereditary | <genetics> Transferred via genes from parent to child. (16 Dec 1997) |