| AR | 1) Aortic Regurgitation = AI Echo소견 &... |
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| GD | gastroduodenal; Gaucher disease; general diagnostics; general dispensary; gestational day; Gianotti ... |
| LAK T cells | Lymphokine Activated Killer T cells |
| SRC | sedimented red cells; sheep red cells |
| UC | ulcerative colitis; ultracentrifugal; umbilical cord; unchanged; unclassifiable; unconscious; undiff... |
| GD | Gaucher disease |
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| CHO-cells | Chinese Hamster Ovary cells |
| PC12 cells | phaeochromocytoma cells |
| AFC | Ab forming cells |
| APC | Ag presenting cells |
| Gaucher cells | Large, finely and uniformly vacuolated cell's derived from the reticuloendothelial system, and found especially in the spleen, lymph nodes, liver, and bone marrow of patients with Gaucher's disease; Gaucher cell's contain kerasin (a cerebroside), which accumulates as a result of a genetically determined absence of the enzyme glucosylceramidase. (05 Mar 2000) |
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| gaucher disease | <radiology> Cerebroside lipidosis, autosomal recessive, abnormal accumulation of glucocerebroside, RE system: liver, spleen, lymph nodes, CNS neurons, skeletal disorders, avascular necrosis, Erlenmeyer flask deformity, resorption of trabeculae, lytic/sclerotic changes, hepatosplenomegaly Cf: Niemann-Pick disease (12 Dec 1998) |
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| Gaucher disorder | <disease> A chronic congenital disease of lipid metabolism caused by a deficiency of the beta-glucocerebrosidase enzyme. The defect is most common in Ashkenazi Jews. Clinical features are hepatosplenomegaly (enlargement of liver and spleen) and in severe early onset forms of the disease, with neurological dysfunction. Inheritance: autosomal recessive. (27 Sep 1997) |
| Gaucher, Philippe | <person> French physician, 1854-1918. See: Gaucher cells, Gaucher's disease, pseudo-Gaucher cell. (05 Mar 2000) |
| Gaucher's disease | <disease> A chronic congenital disease of lipid metabolism caused by a deficiency of the beta-glucocerebrosidase enzyme. The defect is most common in Ashkenazi Jews. Clinical features are hepatosplenomegaly (enlargement of liver and spleen) and in severe early onset forms of the disease, with neurological dysfunction. Inheritance: autosomal recessive. (27 Sep 1997) |
| gaucher's disease, type 1 | A progressive genetic disease caused by a defect in an enzyme. The enzyme, called glucocerebrosidase, is needed to break down the chemical glucocerebroside. The enzyme defect in persons with Gaucher's disease (GD) leads to the accumulation of glucocerebroside in the spleen, liver, and lymph nodes. The most common early sign is enlargement of the spleen (located in the upper left abdomen). Other signs include low red blood cell counts (anaemia), a decrease in blood clotting cells (platelets), increased pigmentation of the skin, and a yellow fatty spot on the white of the eye (a pinguecula). Severe bone involvement can lead to pain and collapse of the bone of the hips, shoulders, and spine. The GD gene is on chromosome 1. The disease is a recessive trait. Both parents carry a GD gene and transmit it for their child with the disease. The parents' risk of a child with the disease is 1 in 4 with each pregnancy. This type of Gaucher's disease (noncerebral juvenile Gaucher's disease) is most common in Ashkenazi Jews (of European origin) and is the most common genetic disease among Jews in the United States. (12 Dec 1998) |
| pseudo-Gaucher cell | A plasma cell, microscopically resembling a Gaucher cell, found in the bone marrow in some cases of multiple myeloma. (05 Mar 2000) |
| disease, gaucher's type 1 | A progressive genetic disease caused by a defect in an enzyme. The enzyme, called glucocerebrosidase, is needed to break down the chemical glucocerebroside. The enzyme defect in persons with Gaucher's disease (GD) leads to the accumulation of glucocerebroside in the spleen, liver, and lymph nodes. The most common early sign is enlargement of the spleen (located in the upper left abdomen). Other signs include low red blood cell counts (anaemia), a decrease in blood clotting cells (platelets), increased pigmentation of the skin, and a yellow fatty spot on the white of the eye (a pinguecula). Severe bone involvement can lead to pain and collapse of the bone of the hips, shoulders, and spine. The GD gene is on chromosome 1. The disease is a recessive trait. Both parents carry a GD gene and transmit it for their child with the disease. The parents' risk of a child with the disease is 1 in 4 with each pregnancy. This type of Gaucher's disease (noncerebral juvenile Gaucher's disease) is most common in Ashkenazi Jews (of European origin) and is the most common genetic disease among Jews in the United States. (12 Dec 1998) |
| absorptive cells of intestine | Cell's on the surface of villi of the small intestine and the luminal surface of the large intestine that are characterised by having microvilli on their free surface. (05 Mar 2000) |
| air cells | Air-containing spaces in the skull. See: pulmonary alveolus. (05 Mar 2000) |
| air cells of auditory tube | Occasional small air cells in the inferior wall of the auditory tube, near the tympanic orifice, communicating with the tympanic cavity. Synonym: cellulae pneumaticae tubae auditivae, air cells of auditory tube. (05 Mar 2000) |
| Alpha cells | Alpha cell's of pancreas or of anterior lobe of hypophysis. (05 Mar 2000) |
| alpha cells of anterior lobe of hypophysis | Acidophil cell's that constitute about 35% of the cell's of the anterior lobe. There are two varieties: one that elaborates somatotropin, another that elaborates prolactin. (05 Mar 2000) |
| alpha cells of pancreas | Cell's of the islets of Langerhans that secrete glucagon. (05 Mar 2000) |
| amniogenic cells | Cell's from which the amnion develops. (05 Mar 2000) |
| anabiotic cells | Cell's that are capable of resuscitation after apparent death; the existence of anabiotic tumour cell's is postulated to explain the recurrence of a cancer after a very long symptomless period following operation. (05 Mar 2000) |
| Gaucher cells, disease (splenomegaly) |
see under cell and disease.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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