| BHV | bovine herpes virus |
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| BK | below the knee; bovine kidney [cells]; bradykinin |
| BLSD | bovine lumpy skin disease |
| BLV | blood volume; bovine leukemia virus |
| BMD | Becker's muscular dystrophy; Boehringer Mannheim Diagnostics; bone marrow depression; bone mineral d... |
| enteric cytopathogenic bovine orphan virus | Former name for early isolates of bovine enteroviruses. Synonym: enteric cytopathogenic bovine orphan virus. (05 Mar 2000) |
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| enzootic bovine leukosis | A lymphoid neoplastic disease in cattle caused by the bovine leukaemia virus. Enzootic bovine leukosis may take the form of lymphosarcoma, malignant lymphoma, or leukaemia but the presence of malignant cells in the blood is not a consistent finding. (12 Dec 1998) |
| ephemeral fever virus, bovine | The type species of ephemerovirus causing disease in cattle. Transmission is by haematophagous arthropods and the virus has been isolated from both culicoides and mosquitoes. (12 Dec 1998) |
| epizootic bovine abortion | An infectious disease of cattle transmitted by the tick Ornithodoros coriaceus and manifested as abortion or weak calves at birth; occurs in the foothills of California, Nevada, and Oregon. Synonym: foothill abortion. (05 Mar 2000) |
| trypanosomiasis, bovine | Infection in cattle caused by various species of trypanosomes. (12 Dec 1998) |
| tuberculosis, bovine | An infection of cattle caused by mycobacterium bovis. It is transmissible to man and other animals. (12 Dec 1998) |
| lentiviruses, bovine | A subgenus of lentivirus comprising viruses that produce multi-organ disease with long incubation periods in cattle. (12 Dec 1998) |
| abelson leukaemia virus | A defective murine leukaemia virus capable of transforming lymphoid cells and producing a rapidly progressing lymphoid leukaemia after superinfection with friend, moloney, or rauscher virus. (12 Dec 1998) |
| Abelson murine leukaemia virus | A retrovirus belonging to the Type C retrovirus group subfamily (family Oncovirinae) which is associated with leukaemia and produces in vitro transformation of mouse cells. (05 Mar 2000) |
| accelerated phase of leukaemia | Refers to chronic myelogenous leukaemia that is progressing. The number of immature, abnormal white blood cells in the bone marrow and blood is higher than in the chronic phase, but not as high as in the blast phase. (12 Dec 1998) |
| acute granulocytic leukaemia | <haematology> A form of leukaemia which is characterised by the proliferation of immature white blood cells (granulocytes) in the bloodstream. Occurs primarily in adults and in infants under 1 year of age. Complications include abnormal bleeding and susceptibility to infections. Symptoms include fatigue, weight loss, fevers, weakness, pallor, bone pains, bleeding gums, nosebleeds, easy bruising, enlarged lymph nodes and joint pains. Treatment includes chemotherapy and/or bone marrow transplant. Origin: Gr. Haima = blood (27 Sep 1997) |
| acute leukaemia | <haematology> A rapidly progressive cancer of the blood of sudden onset and characterised by the uncontrolled proliferation of immature blood cells which take over the bone marrow and spill into the blood stream. If left untreated is fatal within a few weeks or months. See: acute lymphoblastic leukaemia, acute myeloid leukaemia. Origin: Gr. Haima = blood (11 Nov 1997) |
| acute lymphoblastic leukaemia | <haematology> A rapidly progressing cancer of the blood affecting the type of white blood cell known as lymphocytes. Approximately 650 new cases are diagnosed every year in the UK and it is the most common form of childhood leukaemia. Acronym: ALL Origin: Gr. Haima = blood (11 Nov 1997) |
| acute lymphocytic leukaemia | <radiology> 95% of cases of leukaemia in children, bone changes in 50-70% of kids (vs. 10% in adults); seen as early as 1 month after onset of symptoms, wrists and knees most commonly affected, bony defects: metaphyseal radiolucent bands! (similar findings in scurvy, JRA, syphilis), osteolytic lesions, periosteal reaction, osteosclerosis (12 Dec 1998) |
| acute monocytic leukaemia | <haematology> The most common translocation in this disorder of poorly differentiated monocytic cells involves chromosome region 11q in a large percentage of cases. The translocation involves a cellular oncogene, c-ets which is mapped to the 11q23-24 region. The most common translocations reported are t(6;11), t(9;11), t(11;17) and t(11;19), of which t(9;11) (p21-22;q23) is by far the most frequently detected and implicated in acute myeloid leukaemia. The cells express CD14 surface antigen, which is diagnostic of monocytic cells. Acronym: AML Classification: FAB M5 (07 Apr 1998) |
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