| 영문 | fetal assessment | 한글 | 태아사정 |
|---|---|---|---|
| 설명 | 임신 중이나 분만 중의 태아의 상태를 알아보는 것을 태아감시라고 한다. 여기에는 여러 가지 방법이 있는데 크게 분만전 태아감시와 분만중 태아감시로 크게 나눈다. 1. 분만전태아감시: 분만하기 이전의 태아의 상태를 검사하는 방법으로 다음과 같은 여러 가지 방법이 있다. ① 양수천자: 주사기를 이용해서 산모의 배를 통해서 양수를 얻어서 분석하여 태아의 상태를 알아보는 방법. 임신 15주 이상에서 실시할 수 있다. ② 탯줄천자: 초음파검사를 실시하여 영상을 보면서 탯줄 속에 바늘을 넣어서 그 곳의 혈관을 찾아 혈액을 채취하여 검사하는 방법. 아주 위험할 것 같지만 상당히 안전한 것으로 되어 있다. 다른 검사에 비해서 검사에 많은 기술이 필요하지만 아주 많은 정보를 제공해 준다. ③ 비스트레스검사(nonstress test) : 태아도 자궁 속에서 운동을 한다. 그리고 정상적으로 태아가 자궁 속에서 운동을 할 경우에는 태아의 심장 박동이 빨라지게 된다. 태아의 운동과 태아의 심장박동을 동시에 감시하여 운동시에 태아의 심장박동이 빨라지는 가를 알아보는 것이다. |
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| 영문 | fetal alcohol syndrome | 한글 | 태아알코올증후군 |
|---|---|---|---|
| 설명 | 임신기간 중 만성적으로 알코올을 섭취한 여자에게서 태어난 영아에게 나타나는 형태발생의 이상을 나타내는 증후군으로서 위턱뼈발육부전, 앞머리와 아래턱의 돌출, 짧은검열, 작은안구증, 눈구석주름, 심한 성장지연, 정신지체 등을 나타낸다. |
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| 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... |
| EFM | elderly fibromyalgia; electronic fetal monitoring; external fetal monitor |
| FE | fatty ester; fecal emesis; fetal erythroblastosis; fetal erythrocyte; fluid extract; fluorescent ery... |
| FH | facial hemihyperplasia; familial hypercholesterolemia; family history; fasting hyperbilirubinemia; f... |
| 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) |
| congenital ankyloblepharon | Congenital adhesion of the upper and lower eyelid by bands of tissue. Synonym: filiform adnatum. Origin: ankylo-+ G. Blepharon, eyelid (05 Mar 2000) |
| congenital antithrombin III deficiency | Antithrombin III is a protein which stimulates the removal of blood clots in the bloodstream. Small blood clots form normally within the bloodstream, but are normally dissolved via the bodys antithrombin III. The deficiency of antithrombin III will result in an increased risk for blood clot formation causing organ damage. This is an inherited as a autosomal dominant trait. Inheritance: autosomal dominant. (27 Sep 1997) |