| 영문 | cardiac arrest | 한글 | 심장정지 |
|---|---|---|---|
| 설명 | 심장박동이 정지해서 심장이 혈액을 방출할 수 없게된 상태를 말한다. 모든 심근이 수축하지 않고 심장이 완전히 정지된 상태의 ‘심장정지’와 심근이 불규칙-무질서한 수축을 하지만, 박동으로서 혈액은 말초로 방출할 수 없는 상태의 ‘심실잔떨림’이 있다. 임상적으로는 뇌가 비가역적인 변화를 받는 순환기능상실을 심장정지라고 부르고 있다. |
||
| 영문 | cardiac catherization | 한글 | 심장카테테르법, 심도관법 |
|---|---|---|---|
| 설명 | 가느다란 관을 혈관을 통해 심장에 넣어서 여러 가지 진단에 유용한 검사를 하거나 치료를 행하는 것. |
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| CM | California mastitis [test]; calmodulin; capreomycin; carboxymethyl; cardiac murmur; cardiac muscle; ... |
|---|---|
| CP | candle power; capillary pressure; cardiac pacing; cardiac performance; cardiopulmonary; caudate puta... |
| CA | anterior commissure [Lat. commissura anterior]; calcium antagonist; California [rabbit]; cancer; Can... |
| CD | cadaver donor; canine distemper; canine dose; carbohydrate dehydratase; carbon dioxide; cardiac dise... |
| POSSUM | Pictures of Standard Syndromes and Undiagnosed Malformations |
| 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) |
| congenital aplasia of thymus | diGeorge syndrome |
| congenital aplastic anaemia | <haematology> A rare inherited type of aplastic anaemia which carries an increased risk to the patient of developing leukaemia. May be treated by bone marrow transplant. Origin: Gr. Haima = blood (13 Nov 1997) |
| congenital atonic pseudoparalysis | Atonic pseudoparalysis of congenital origin (neither familial nor hereditary), observed especially in infants and characterised by absences of muscular tone only in muscles innervated by the spinal nerves. Synonym: congenital atonic pseudoparalysis, myatonia congenita, Oppenheim's disease, Oppenheim's syndrome. An indefinite term for a number of congenital neuromuscular disorders that cause generalised myotonia in young children, and that have a benign course (static or regressive). (05 Mar 2000) |
| congenital baldness | Absence of all hair at birth, associated with psychomotor epilepsy; autosomal dominant inheritance. Synonym: congenital baldness, hypotrichiasis. (05 Mar 2000) |
| congenital bronchiectasis | Persistent and progressive dilation of bronchi or bronchioles as a consequence of inflammatory disease (lung infections), obstruction (tumour) or congenital abnormality (for example cystic fibrosis). Although rarely congenital, it is most often an acquired condition in childhood. (27 Sep 1997) |
| congenital cardiomyopathy | <radiology> Endocardial fibroelastosis, myocarditis, glycogen storage disease (Pompe's), anomalous origin of left coronary artery from pulmonary artery (12 Dec 1998) |
| congenital cataract | A cataract or clouding or the lens of the eye, that occurs in the foetus at some time during pregnancy. Children with Down's syndrome and galactosaemia have an increased incidence of congenital cataracts. Treatment includes cataract removal and the insertion of an artificial lens. (27 Sep 1997) |
| congenital cerebellar atrophy | Familial disorder that causes degeneration of various cells in the cerebellum. Two types are recognised, one in which the granular layer cells degenerate, the other in which the Purkinje cells degenerate. (05 Mar 2000) |