| 영문 | Golgi body | 한글 | 골지체 |
|---|---|---|---|
| 설명 | 세포내의 세포질 소기관. 골지장치라고도 한다. 1898년 이탈리아의 C. 골지에 의해 올빼미의 신경세포체에서 발견되었으며, 이후 다른 세포에서, 또 근래에는 식물세포에서도 발견되고 있다. 전자 현미경에 의한 연구에서 골지체에 해당되는 부분은 층상구조-꽈리구조-알갱이 구조의 세가지로 되어 있으며, 이것을 골지역이라 한다. 그 작용은 명확하지는 않으나 샘세포의 소포체에서 합성된 분비물이 골지역에서 농축되어 분비과립이 되고, 그 과립의 외측에 막이 형성된다고 생각되고 있다. 골지체는 막구조를 주로 하기 때문에 인지질과 단백질을 많이 가지며 알칼리성 포스파타아제-비타민 C-카로틴 등을 함유한다. |
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| 영문 | basal body temperature | 한글 | 기초체온 |
|---|---|---|---|
| 설명 | 음식-운동-정신감동 등 체온에 영향을 줄 만한 여러 조건을 피하여 몸과 마음이 안정되었을 때 잰 체온, 보통 아침에 눈을 뜬 직후에 재며, 여성의 경우 월경 주기에 따라 달라지므로 수태 조절이나 자궁, 난소의 병 진단에 응용한다. 6~8시간의 안정된 수면을 취한 후 아침 일찍 깨어나, 잠자리에서 나오기 전에 체온계를 입에 물어서 측정한다. 미묘한 체온의 차이를 측정하는 것이므로 여성체온계를 사용하는 것이 좋다. 이 여성체온계의 수은구부를 혀의 아랫면에 끼우고서 입을 가볍게 다물고 약 5분 동안 있다가 측정하면 된다. 정상적인 기초체온은 복잡한 성주기의 변화를 보이기 때문에 월경주기에 관한 각종 진단을 비롯하여 임신-유산-이상임신의 진단과 수태조절 등에 응용하는 등 여러 가지 효과적인 자료가 된다. |
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| 영문 | planes of body | 한글 | 인체의 면 |
|---|---|---|---|
| 설명 | 인체를 여러 개로 나누는 면이 있는데, 크게 시상면(sagittal plane), 관상면(coronal plane), 수평면(horizontal plane)으로 나눌 수 있다. 시상면은 인체를 좌우로, 관상면은 앞뒤로, 수평면은 위아래로 가르는 면이다. |
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| CHBA | congenital Heinz body hemolytic anemia |
|---|---|
| CHBHA | congenital Heinz body hemolytic anemia |
| IB | idiopathic blepharospasm; immune body; inclusion body; index of body build; infectious bronchitis; I... |
| LB | lamellar body; large bowel; left breast; left bronchus; left bundle; left buttock; leiomyoblastoma; ... |
| TBS | total body solids; total body solute; total body surface; total burn size; Townes-Brocks syndrome; t... |
| ACD | Anaemia of chronic disease |
|---|---|
| AIHA | Auto-immune haemolytic anaemia |
| AHA | autoimmune haemolytic anaemia |
| CAV | Chicken Anaemia Virus |
| CAA | Chicken anaemia agent |
| Heinz body anaemia | A congenital haemolytic anaemia, due to autosomal inheritance of one of many unstable haemoglobins. The anaemia is of variable severity and characterised by the presence in vivo or in vitro of Heinz bodies. (05 Mar 2000) |
|---|
| Heinz body test | <haematology, investigation> A test for glucose-6-phosphate dehydrogenase-deficient red blood cells; an oxidant (acetylphenylhydrazine) is added to blood; after incubation at 37캜, glucose-6-phosphate dehydrogenase-deficient samples exhibit more than 30% Heinz bodies. (05 Mar 2000) |
|---|---|
| Heinz-Ehrlich body | A round oxyphil body found in the red blood cell in case of haemocytolysis due to a specific blood poison. Synonym: Heinz-Ehrlich body. (05 Mar 2000) |
| heinz bodies | Coccoid inclusion bodies resulting from oxidative injury to and precipitation of haemoglobin, seen in the presence of certain abnormal haemoglobins and erythrocytes with enzyme deficiencies. (12 Dec 1998) |
| Heinz, Robert | <person> German pathologist. Lived: 1865-1924. See: Heinz bodies, Heinz body test, Heinz-Ehrlich body, Heinz body anaemia. (05 Mar 2000) |
| 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) |
| anaemia, dyserythropoietic, congenital | A familial disorder characterised by anaemia with multinuclear erythroblasts, karyorrhexis, asynchrony of nuclear and cytoplasmic maturation, and various nuclear abnormalities of bone marrow erythrocyte precursors. Type II is the most common of the 3 types of congenital dyserythropoietic anaemia; it is often referred to as hempas, based on the hereditary erythroblast multinuclearity with positive acidified serum test. (12 Dec 1998) |
| anaemia gravis | <haematology> This form of anaemia occurs when the bone marrow ceases sufficient red and white blood cell production. It may be induced by exposures to high levels of toxic chemicals, radiation and certain drugs. It is generally unresponsive to specific therapy, often accompanied by granulocytopenia and thrombocytopenia, in which the bone marrow may not necessarily be hypocellular or hypoplastic but fails to produce adequate numbers of peripheral blood elements. The term actually is all inclusive and most probably encompasses several clinical syndromes. Origin: Gr. Haima = blood (29 Sep 1997) |
| anaemia, haemolytic | Anaemia due to decreased life span of erythrocytes. (12 Dec 1998) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|