| 영문 | large intestine | 한글 | 큰창자, 대장 |
|---|---|---|---|
| 설명 | 사람의 소화기관은 여러 가지 기관으로 구성되어 있는데, 이중 창자관계는 식도, 위, 작은창자와 큰창자로 구성되어 있다. 입으로 먹어서 잘게 분해된 음식은 식도를 거쳐, 위에서 단백질 등이 소화되고, 샘창자에서 이자에서 분비된 소화효소에 의해 소화, 일부 흡수된 후, 대부분의 영양분은 작은창자에서 흡수된다. 큰창자는 주로 물과 미량원소, 전해질의 흡수에 이용되며, 작은창자에서 내려온 분비물을 저장해 두었다가 큰창자를 거쳐 항문으로 대변을 배설하게 된다. 큰창자는 그 위치에 따라 3부분으로 구성되어지며, 막창자, 잘룩창자 그리고 곧창자이다. 잘룩창자은 다시 오름창자, 가로창자, 내림창자로 이루어져 있으며, 이것은 구불창자란 말은 S자 모양으로 굽어져 있다는 말이다)으로 이어져 곧창자장을 거쳐 항문으로 연결된다. |
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| CAV | congenital absence of vagina; congenital adrenal virilism; constant angular velocity; croup-associat... |
|---|---|
| CC | calcaneal-cuboid; calcium cyclamate; cardiac catheterization; cardiac contusion; cardiac cycle; card... |
| CHA | Canadian Hospital Association; Catholic Health Association; Chinese hamster; chronic hemolytic anemi... |
| CHD | Chediak-Higashi disease; childhood disease; chronic hemodialysis; congenital or congestive heart dis... |
| GnRH | Gonadotropin Releasing Hormone [HP 1898, 2034] = LHRH = Go... |
| law of intestine | Contraction above and relaxation below a stimulated point in the intestine. Synonym: law of intestine. (05 Mar 2000) |
|---|---|
| adrenal hyperplasia, congenital | A group of inherited disorders of adrenal steroidogenesis, the physical expression of which varies with the sex of the patient, the severity of the congenital enzyme defect, and the age at which the defect makes its presence felt. The most common form, the simple virilizing form, is due to a 21-hydroxylase deficiency. There is also a salt-losing form (a more complete 21-hydroxylase deficiency), a hypertensive form (11-hydroxylase deficiency), a 17-hydroxylase deficiency form, a desmolase deficiency form, and a 3-beta-hydroxysteroid deficiency form. (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, haemolytic, congenital | Haemolytic anaemia due to various intrinsic defects of the erythrocyte. (12 Dec 1998) |
| anaemia, haemolytic, congenital nonspherocytic | Any one of a group of congenital haemolytic anaemias in which there is no abnormal haemoglobin or spherocytosis and in which there is a defect of glycolysis in the erythrocyte. In some cases, pyruvate kinase deficiency has been demonstrated; in other cases, glucose-6-phosphate dehydrogenase deficiency has been demonstrated. (12 Dec 1998) |
| bovine congenital ataxia | An autosomal recessive ataxia seen in several European breeds of cattle. (05 Mar 2000) |
| bullous congenital ichthyosiform erythroderma | Diffusely red, eroded skin at birth, with subsequent scaling, tending to improve in later life, characterised by generalised epidermolytic hyperkeratosis and autosomal dominant inheritance. See: epidermolytic hyperkeratosis. Synonym: generalised epidermolytic hyperkeratosis, ichthyismus hystrix, ichthyosis hystrix. (05 Mar 2000) |
| pain insensitivity, congenital | Absence of sensibility to pain or inability to feel pain. The condition is present at birth. (12 Dec 1998) |
| rubella syndrome, congenital | Transplacental infection of the foetus with rubella usually in the first trimester of pregnancy, as a consequence of maternal infection, resulting in various developmental abnormalities in the newborn infant. They include cardiac and ocular lesions, deafness, microcephaly, mental retardation, and generalised growth retardation. (12 Dec 1998) |
| congenital | <embryology> Existing at and usually before, birth, referring to conditions that are present at birth, regardless of their causation. Origin: L. Congenitus = born together (18 Nov 1997) |
| congenital absence of pulmonary valve | <radiology> BIG central pulmonary arteries, big RV (12 Dec 1998) |
| congenital adrenal hyperplasia | <endocrinology> A genetic disorder present at birth characterised by a deficiency of the hormones aldosterone and cortisol and an overproduction of male sex hormones (androgens). In males this may manifest as enlarged penis, small testes and early development of masculine characteristics. In females features include ambiguous genitalia, failure to menstruate, deep voice and excessive hair. Origin: Gr. Plassein = to form (27 Sep 1997) |
| congenital afibrinogenaemia | <biochemistry> A below normal level of fibrinogen in the plasma. Fibrinogen (factor II) is one of the proteins involved in the formation of a blood clot. This condition may be congenital or acquired (for example disseminated intravascular coagulation, multiple blood transfusions). Origin: Gr. Haima = blood (27 Sep 1997) |
| congenital amputation | Amputation produced in utero; attributed to the pressure of constricting bands (amniotic); autosomal recessive inheritance. Synonym: amniotic amputation, amputation, birth amputation, intrauterine amputation, spontaneous amputation. (05 Mar 2000) |
| congenital anaemia | <haematology> A condition which develops in the foetus due to an incompatibility between the mother's blood type (RH factor) and the baby's. Maternal antibodies, which enter the foetal circulation during delivery attack the baby's red blood cells leading to haemolysis (rupture of the cells). Symptoms include an infant with an enlarged liver and spleen, swelling, jaundice and anaemia. (27 Sep 1997) |