| BART | blood-activated recalcification time |
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| Bart's syndrome | <syndrome> A form of epidermolysis bullosa with blistering of the extremities and intertriginous areas, erosions of the mouth, and deformed nails; probably autosomal dominant; there is often spontaneous improvement with no residual scarring. (05 Mar 2000) |
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| Bart, Bruce | <person> U.S. Dermatologist, *1936. See: Bart's syndrome. (05 Mar 2000) |
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| haemoglobin Bart's | A Hb homotetramer (all four polypeptides identical) of formula g4, found in the early embryo and in alpha-thalassaemia 2; not effective in oxygen transport; does not display a Bohr effect. (05 Mar 2000) |
| Bart's hemoglobin |
A form of thalassemia in which the affected individual carries two copies of the alpha thalassemic globin gene from each parent. This condition causes erythroblastosis fetalis, which leads to intrauterine death or death within
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| Bart's s. |
a form of epidermolysis bullosa dystrophica inherited as an autosomal dominant trait, characterized by congenital localized absence of the skin with blister formation as a result of mechanical trauma and nail dystrophy.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| Bart's syndrome |
see under syndrome.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
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