| 영문 | cerebral aneurysm | 한글 | 뇌동맥류, 뇌동맥자루 |
|---|---|---|---|
| 설명 | 뇌의 동맥에 생긴 동맥자루. 임상적으로 중요시되는 이유는 이것이 잘 터져 뇌출혈의 중요한 원인이 되기 때문이다. 대부분의 동맥자루가 출혈을 일으키지만 출혈을 일으키지 않는 경우에는 주위의 뇌 조직의 압박에 의해서 두통이나 발작 등을 일으킬 수 있다. |
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| 영문 | cerebral palsy | 한글 | 뇌성마비 |
|---|---|---|---|
| 설명 | 출생전, 출생시 혹은 출생후의 뇌의 선천기형, 손상 혹은 중추신경계의 병에 의해서 영구적이며, 비진행성인 운동신경 및 정신장애를 일으키는 경우를 뜻한다. 원인은 여러 가지가 있을 수 있으나 조산으로 인한 뇌의 산소공급의 부족, 또는 난산으로 인한 호흡장애 등이 흔한 원인이다. 증상은 대개 비진행성의 뇌 병변으로 인한 운동장애가 대표적인 증상이며 그외에 청력, 시력의 장애, 지능부전, 언어장애, 경련 및 정신장애 등이 동반될 수 있다. |
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| 영문 | cerebral contusion | 한글 | 뇌좌상 |
|---|---|---|---|
| 설명 | 외부에서 기원하는 물리적 충격에 의한 뇌의 물리적 손상. |
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| 영문 | cerebral concussion | 한글 | 뇌진탕 |
|---|---|---|---|
| 설명 | 외부에서 기원하는 물리적 충격으로 인해 뇌의 물리적 손상없이 일어나는 뇌의 기능 장애. 일시적으로 무의식, 반사소실, 등이 나타나지만 결국은 아무 후유증없이 정상으로 돌아온다. |
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| 영문 | cerebral cortex | 한글 | 대뇌겉질 |
|---|---|---|---|
| 설명 | 대뇌의 표면부위를 대뇌겉질이라고도 한다. 대개 얕은회색질(superficial gray matter)와 동의어로 쓰인다. 회색질이란 대뇌의 표면에 신경세포가 모여있는 곳으로 회색을 띠는 부분을 말한다. 이와는 대조적으로 백색질이란 신경세포가 내는 신경섬유가 분포하는 곳이며 대뇌에서 회색질의 안쪽에 존재한다. 참고로 말하면 척수에서는 대뇌와 반대로 회색질 안쪽에 존재하고 백색질이 밖에 존재한다. 즉 척수에서는 신경세포가 척수의 안쪽에 존재하고 바깥쪽에 그 신경세포가 내는 신경섬유가 존재한다. |
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| CA | anterior commissure [Lat. commissura anterior]; calcium antagonist; California [rabbit]; cancer; Can... |
|---|---|
| CPC | central posterior curve; cerebellar Purkinje cell; cerebral palsy clinic; cerebral performance categ... |
| CT | calcitonin; calf testis; cardiac tamponade; cardiothoracic [ratio]; carotid tracing; carpal tunnel; ... |
| TCI | total cerebral ischemia; transient cerebral ischemia; transcobalamin I |
| CAS | calcarine sulcus; calcific aortic stenosis; Cancer Attitude Survey; carbohydrate-active steroid; car... |
| ovarian cysts | General term for cysts and cystic diseases of the ovary. (12 Dec 1998) |
|---|---|
| enterogenous cysts | Mediastinal cysts derived from cells sequestered from the primitive foregut; may be classified histologically as bronchogenic, oesophageal, or gastric. (05 Mar 2000) |
| jaw cysts | Saccular lesions lined with epithelium and contained within pathologically formed cavities in the jaw; also nonepithelial cysts (pseudocysts) as they apply to the jaw, e.g., traumatic or solitary cyst, static bone cavity, and aneurysmal bone cyst. True jaw cysts are classified as odontogenic or nonodontogenic. (12 Dec 1998) |
| foregut cysts | <radiology> Bronchogenic and enteric cysts: more common on the right, neurenteric cysts: associated with vertebral anomalies, enteric cysts: may contain acid-secreting gastric mucosa;, confirm with TcO4 scan (12 Dec 1998) |
| 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) |