| CoR | Congo red |
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| CR | calculation rate; calculus removed; calorie-restricted; cardiac rehabilitation; cardiac resuscitatio... |
| CR | Congo Red |
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| C-CHF | Crimean-Congo hemorrhagic fever |
| ACD | Anaemia of chronic disease |
| AIHA | Auto-immune haemolytic anaemia |
| AHA | autoimmune haemolytic anaemia |
| Belgian Congo anaemia | A form of anaemia occurring in natives of Zaire (formerly the Belgian Congo), with associated oedema of subcutaneous tissues, depigmented regions in the skin, and various gastrointestinal disturbances; thought to result from deficiencies in nutrition. Synonym: Belgian Congo anaemia. (05 Mar 2000) |
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| Bennhold's Congo red stain | <technique> An amyloid stain useful for amyloid detection in pathologic tissue; gives red staining of amyloid; also induces green birefringence to amyloid under polarised light. (05 Mar 2000) |
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| congo | A republic in central africa lying between gabon and democratic republic of the congo. Its capital is brazzaville. It became a territory of french equatorial africa in 1910, a french overseas territory in 1946, an autonomous republic within the french community in 1958, and achieved independence in 1960. The country takes its name from the congo river running through it: the bantu name for the river means mountain, with reference to the local topography. (12 Dec 1998) |
| congo red | <chemical> An odourless, dark red or reddish brown powder which decomposes on exposure to acid fumes. It is used as a diagnostic aid in amyloidosis, and has been used as an antihemolytic and detoxicant. Pharmacological action: dyes. Chemical name: 1-Naphthalenesulfonic acid, 3,3'-((1,1'-biphenyl)-4,4'-diylbis(azo))bis(4-amino-, disodium salt (12 Dec 1998) |
| Crimean-Congo haemorrhagic fever | A form of haemorrhagic fever distinct from Omsk haemorrhagic fever, occurring in central Russia, transmitted by species of the tick Hyalomma, and caused by Crimean-Congo haemorrhagic fever virus, a member of the Bunyaviridae family; horses are the chief reservoir of human infection; characterised by abrupt onset, high fever, headache, myalgia, widespread petechial haemorrhagic lesions, gastrointestinal bleeding, high fatality rate. Synonym: African tick fever. (05 Mar 2000) |
| Crimean-Congo haemorrhagic fever virus | A virus of the genus Nairovirus (family Bunyaviridae) from Africa and the southern USSR, carried by ticks (Hyalomma and Amblyomma) and found in human blood; the cause of Crimean-Congo haemorrhagic fever. (05 Mar 2000) |
| haemorrhagic fever virus, crimean-congo | The type species of nairovirus of the family bunyaviridae isolated from febrile patients in africa. It is primarily transmitted by ticks and causes a severe, often fatal disease in humans. (12 Dec 1998) |
| democratic republic of the congo | A republic in central africa, south of the central african republic and north of angola and zambia. Its name changes bespeak its history: 1885-1908 congo free state, 1908-60 belgian congo, 1960-71 democratic republic of the congo, 1971-97 zaire. It changed its name back to democratic republic of the congo in 1997. The name zaire is an alternate name for the congo river from nzai, a kikongo dialect form of nazdi, river. (12 Dec 1998) |
| achlorhydric anaemia | A form of chronic hypochromic microcytic anaemia associated with achlorhydria or achylia gastrica; observed most frequently in women in the third to fifth decades. Synonym: Faber's anaemia, Faber's syndrome. (05 Mar 2000) |
| achrestic anaemia | A form of chronic progressive macrocytic anaemia that can be fatal in which the changes in bone marrow and circulating blood closely resemble those of pernicious anaemia, but in which there is only transient or no response to therapy with vitamin B12; glossitis, gastrointestinal disturbances, central nervous system disease, and pyrexia are not observed, and there is only little bleeding or haemolysis. Origin: G. A-priv. + chresis, a using (05 Mar 2000) |
| acquired haemolytic anaemia | Nonhereditary acute or chronic anaemia associated with or caused by extracorpuscular factors, e.g., certain infectious agents, chemicals (including autoantibodies or therapeutic agents), burns, toxic materials from higher plant and animal forms (including snake venoms). (05 Mar 2000) |
| addisonian anaemia | <haematology> A form of anaemia (low red blood cell counts) that results when the bone marrow fails to produce adequate numbers of red blood cells due to a deficiency in vitamin B12. Intrinsic factor, necessary for normal B12 absorption, may be the underlying cause for B12 deficiency if is not produced in the gastric glands (in the stomach). Origin: Gr. Haima = blood (27 Sep 1997) |
| Addison's anaemia | <haematology> A form of anaemia (low red blood cell counts) that results when the bone marrow fails to produce adequate numbers of red blood cells due to a deficiency in vitamin B12. Intrinsic factor, necessary for normal B12 absorption, may be the underlying cause for B12 deficiency if is not produced in the gastric glands (in the stomach). Origin: Gr. Haima = blood (27 Sep 1997) |
| anaemia | <haematology> Too few red blood cells in the bloodstream, resulting in insufficient oxygen to tissues and organs. Origin: Gr. Haima = blood (16 Dec 1997) |
| anaemia, aplastic | A form of anaemia in which the bone marrow fails to produce adequate numbers of peripheral blood elements. (12 Dec 1998) |
| anaemia, Cooley's | Better known today as thalassaemia (or as beta thalassaemia or thalassaemia major).The clinical picture of this important type of anaemia was first described in 1925 by the paediatrician Thomas Benton Cooley. Another name for the disease is Mediterranean anaemia. The name thalassaemia was coined by the Nobel Prise winning pathologist George Whipple and the professor of paediatrics Wm Bradford at Univ. Of Rochester because thalassa in Greek means the sea (like the Mediterrranean Sea) + -aemia means in the blood so thalassaemia means sea in the blood. Thalassaemia is not just one disease. It is a complex contingent of genetic (inherited) disorders all of which involve underproduction of haemoglobin, the indispensable molecule in red blood cells that carries oxygen. The globin part of normal adult haemoglobin is made up of 2 alpha and 2 beta polypeptide chains. In beta thalassaemia, there is a mutation (change) in both beta globin chains leading to underproduction (or absence) of beta chains, underproduction of haemoglobin, and profound anaemia. The gene for beta thalassaemia is relatively frequent in people of Mediterranean origin (for example, from Italy and Greece). Children with this disease inherit one gene for it from each parent. The parents are carriers (heterozygotes) with just one thalassaemia gene, are said to have thalassaemia minor, and are essentially normal. Their children affected with beta thalassaemia seem entirely normal at birth because at birth we still have predominantly foetal haemoglobin which does not contain beta chains. The anaemia surfaces in the first few months after birth and becomes progressively more severe leading to pallor and easy fatiguability, failure to thrive (grow), bouts of fever (due to infections) and diarrhoea. Treatment based on blood transfusions is helpful but not curative. Gene therapy will, it is hoped, be applicable to this disease. (12 Dec 1998) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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