| 영문 | infectious disease | 한글 | 감염병 |
|---|---|---|---|
| 설명 | 바이러스로부터 기생충 크기까지의 생물을 원인으로 하는 병. 원인은 접촉전염성이며, 병원에서 감염되는 경우도 있다. 감염을 원인균에 따라 분류하면 바이러스, 세균, 클라미디아, 리켓차, 미코박테리움, 곰팡이, 원충, 윤충, 외부기생충 감염으로 나눌 수 있다. |
||
| 영문 | infectious mononucleosis | 한글 | 전염단핵구증 |
|---|---|---|---|
| 설명 | Epstein-Barr 바이러스에 의해서 일어나는 급성 감염병. 발열, 쇠약, 인후통, 간기능장애, 림프절비대, 간지라비대, 말초혈액중의 비정형림프구(단구와 유사한) 및 양세포에 대한 고역가의 응집소를 특징으로 한다. 질병의 경과중 및 회복기간을 통해서 현저한 무력증이 지속된다. 같은 증후군이 원발성 거대세포바이러스감염에도 동반된다. 키스병이라고도 하며, 침에 의한 EB바이러스 감염에 의해 발병한다. |
||
| CD | cadaver donor; canine distemper; canine dose; carbohydrate dehydratase; carbon dioxide; cardiac dise... |
|---|---|
| ICH | idiopathic cortical hyperostosis; infectious canine hepatitis; intracerebral hematoma; intracranial ... |
| IBV | infectious bronchitis vaccine; infectious bronchitis virus |
| IPV | inactivated poliomyelitis vaccine or virus; infectious pustular vaginitis; infectious pustular vulvo... |
| TAR | Thrombocytopenia-Absent Radius |
| cyclic AMP | 3',5'-cyclic adenosine monophosphate |
|---|---|
| cyclic AMP | 3',5'-cyclic monophosphate |
| cyclic GMP | 3',5'-cyclic monophosphate |
| cyclic AMP | Cyclic 3',5' adenosine monophosphate |
| cyclic GMP | Cyclic guanosine 3',5' monophosphate |
| canine infectious cyclic thrombocytopenia | An infection of dogs with the rickettsia Ehrlichia platys characterised by recurrent cyclic thrombocytopenia. (05 Mar 2000) |
|---|
| hepatitis, infectious canine | An adenovirus infection causing fever, oedema, vomiting, and diarrhoea in dogs, especially puppies. In foxes it causes acute encephalitis with convulsions, paralysis, coma, and death. (12 Dec 1998) |
|---|---|
| infectious canine hepatitis | A disease of dogs, caused by canine adenovirus 1, and characterised by fever, depression, loss of appetite, vomiting, bloody diarrhoea, petechial haemorrhages in the gums, pale mucous membranes, and jaundice. Synonym: hepatitis contagiosa canis, Rubarth's disease. (05 Mar 2000) |
| autoimmune thrombocytopenia purpura | <haematology> A rare autoimmune disorder characterised by an acute shortage of platelets with resultant bruising and spontaneous bleeding. The platelet count becomes exceedingly low and spontaneous bleeding from the gums, gastrointestinal tract and nose can be seen. Physical examination may demonstrate enlargement of the spleen. A typical rash occurs to do microscopic haemorrhage of small blood vessels in the skin. Platelet counts under 10,000 can lead to spontaneous haemorrhage into the brain causing death. Treatment with corticosteroids is generally effective. Surgical removal of the spleen (splenectomy) is reserved for some patients. Anti-platelet antibodies are detectable in some cases. It may present in either an acute or a chronic form. Acronym: ITP (20 Sep 2002) |
| radial aplasia-thrombocytopenia syndrome | <syndrome> Aplasia (absence) of the radius (the long bone on the thumb-side of the forearm) and thrombocytopenia (low blood platelets) are key features characterizing this syndrome. There is phocomelia (flipper-limb) with the thumbs always present. The fibula (the smaller bone in the lower leg) is often absent. The risk of bleeding from too few platelets is high in early infancy but lessens with age. The condition is inherited in an autosomal recessive trait with one gene (on a non-sex chromosome) coming from each parent to the child affected with the disease. Alternative names include thrombocytopenia-absent radius syndrome, tar syndrome, and tetraphocomelia-thrombocytopenia syndrome. (12 Dec 1998) |
| haemangioma-thrombocytopenia syndrome | <syndrome> Thrombocytopenia caused by sequestration and destruction of platelets in a large cavernous haemangioma, usually seen in infants, rare in adults (12 Dec 1998) |
| syndrome, radial aplasia-thrombocytopenia | See syndrome, tar. (12 Dec 1998) |
| syndrome, tetraphocomelia-thrombocytopenia | See syndrome, tar. (12 Dec 1998) |
| syndrome, thrombocytopenia-absent radius | See Syndrome, TAR. (12 Dec 1998) |
| idiopathic thrombocytopenia purpura | <haematology> A rare autoimmune disorder characterised by an acute shortage of platelets with resultant bruising and spontaneous bleeding. The platelet count becomes exceedingly low and spontaneous bleeding from the gums, gastrointestinal tract and nose can be seen. Physical examination may demonstrate enlargement of the spleen. A typical rash occurs to do microscopic haemorrhage of small blood vessels in the skin. Platelet counts under 10,000 can lead to spontaneous haemorrhage into the brain causing death. Treatment with corticosteroids is generally effective. Surgical removal of the spleen (splenectomy) is reserved for some patients. Anti-platelet antibodies are detectable in some cases. It may present in either an acute or a chronic form. Acronym: ITP (20 Sep 2002) |
| immune thrombocytopenia | Thrombocytopenia associated with antiplatelet antibodies. See: isoimmune neonatal thrombocytopenia, autoimmune neonatal thrombocytopenia. (05 Mar 2000) |
| isoimmune neonatal thrombocytopenia | Immune thrombocytopenia resulting from maternal-foetal platelet incompatibility. (05 Mar 2000) |
| tetraphocomelia-thrombocytopenia syndrome | <syndrome> Tar stands for thrombocytopenia (low blood platelets) and aplasia (absence) of the radius (the long bone on the thumb-side of the forearm), features characterizing this syndrome. There is phocomelia (flipper-limb) with the thumbs always present. The fibula (the smaller bone in the lower leg) is often absent. The risk of bleeding from too few platelets is high in early infancy but lessens with age. The condition is inherited in an autosomal recessive trait with one gene (on a non-sex chromosome) coming from each parent to the tar child. Alternative names include thrombocytopenia-absent radius syndrome, radial aplasia-thrombocytopenia syndrome, and tetraphocomelia-thrombocytopenia syndrome. (12 Dec 1998) |
| thrombocytopenia | <haematology> A decrease in the number of platelets in the blood, resulting in the potential for increased bleeding and decreased ability for clotting. Origin: Gr. Penia = poverty (18 Nov 1997) |
| thrombocytopenia-absent radius syndrome | <syndrome> Tar stands for thrombocytopenia (low blood platelets) and aplasia (absence) of the radius (the long bone on the thumb-side of the forearm), features characterizing this syndrome. There is phocomelia (flipper-limb) with the thumbs always present. The fibula (the smaller bone in the lower leg) is often absent. The risk of bleeding from too few platelets is high in early infancy but lessens with age. The condition is inherited in an autosomal recessive trait with one gene (on a non-sex chromosome) coming from each parent to the tar child. Alternative names include thrombocytopenia-absent radius syndrome, radial aplasia-thrombocytopenia syndrome, and tetraphocomelia-thrombocytopenia syndrome. (12 Dec 1998) |
| thrombocytopenia purpura | <haematology> In severe thrombocytopenia, bleeding into skin leads to small petechial haemorrhages. Primary thrombocytopenia purpura is of unknown cause but results from an autoimmune mechanism that causes platelet destruction. Secondary thrombocytopenic purpura may result from drug-induced type II hypersensitivity in which platelets coated with antibody to the drug (which is acting as a hapten) are destroyed in a complement mediated reaction. It can also follow a viral upper respiratory infection and may be seen in association with lupus. (15 Oct 1997) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|