| 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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| 영문 | cerebral artery | 한글 | 대뇌동맥 |
|---|---|---|---|
| 설명 | 대뇌의 혈액을 공급하는 동맥. 대뇌의 앞부분의 혈액을 공급하는 앞대뇌동맥(anterior cerebral artery), 중간부위의 혈액을 공급하는 중간대뇌동맥(middle cerebral artery), 뒷부분의 혈액을 공급하는 뒤대뇌동맥(posterior cererbral artery)의 세 가지가 있다. 대뇌는 크게 두 가지 동맥에 의해서 혈액을 공급받는다. 하나는 속목동맥(internal carotid artery)이고 하나는 척추동맥(vertebral artery)이다. 이 동맥들은 좌-우로 두 개씩 쌍을 이루어 뇌에 혈액을 공급한다. 척추동맥은 대동맥에서 나와서 목뼈에 있는 가로돌기구멍을 통해서 머리쪽으로 올라온다. 그리고는 두 개의 좌우 척추가 한 개로 합쳐져서 바닥동맥라는 동맥을 이룬다. 목동맥은 대동맥에서 기시하여 속목동맥과 바깥목동맥으로 나뉜다(나뉘기 이전을 온목동맥이라 한다). 바깥목동맥은 얼굴과 뇌를 제외한 머리의 부위에 혈액을 공급하는 혈관이고, 속목동맥은 뇌에 혈액을 공급한다.   |
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| 영문 | cerebral hemisphere | 한글 | 대뇌반구 |
|---|---|---|---|
| 설명 | 대뇌란 뇌의 가장 큰 부분을 차지하는 곳으로 사고, 운동, 성격, 기억 등의 고차원적인 기능을 행하는 곳이다. 대뇌는 크게 좌, 우 두 개로 나뉘어져 있고 각각을 좌, 우 대뇌반구라고 한다. |
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| HCHWA | hereditary cerebral hemorrhage with amyloidosis |
|---|---|
| CA | anterior commissure [Lat. commissura anterior]; calcium antagonist; California [rabbit]; cancer; Can... |
| CC | calcaneal-cuboid; calcium cyclamate; cardiac catheterization; cardiac contusion; cardiac cycle; card... |
| CM | California mastitis [test]; calmodulin; capreomycin; carboxymethyl; cardiac murmur; cardiac muscle; ... |
| CPC | central posterior curve; cerebellar Purkinje cell; cerebral palsy clinic; cerebral performance categ... |
| hereditary angioedema | A genetic form of angioedema. (angioedema is also referred to as quinke's disease.) persons with it are born lacking an inhibitor protein (called c1 esterase inhibitor) that normally prevents activation of a cascade of proteins leading to the swelling of angioedema. Patients can develop recurrent attacks of swollen tissues, pain in the abdomen, and swelling of the voice box (larynx) which can compromise breathing. The diagnosis is suspected with a history of recurrent angioedema. It is confirmed by finding abnormally low levels of c1 esterase inhibitor in the blood. Treatment options include antihistamines and male steroids (androgens) that can also prevent the recurrent attacks. Also called hereditary angioneurotic oedema. (12 Dec 1998) |
|---|---|
| hereditary angioneurotic oedema | A genetic form of angioedema. (angioedema is also referred to as quinke's disease.) persons with it are born lacking an inhibitor protein (called c1 esterase inhibitor) that normally prevents activation of a cascade of proteins leading to the swelling of angioedema. Patients can develop recurrent attacks of swollen tissues, pain in the abdomen, and swelling of the voice box (larynx) which can compromise breathing. The diagnosis is suspected with a history of recurrent angioedema. It is confirmed by finding abnormally low levels of c1 esterase inhibitor in the blood. Treatment options include antihistamines and male steroids (androgens) that can also prevent the recurrent attacks. Also called hereditary angioedema. (12 Dec 1998) |
| hereditary angio oedema | <biochemistry> Condition in which there seems to be uncontrolled production of C2 kinin because of a deficiency in C1 inhibitor levels. (18 Nov 1997) |
| hereditary areflexic dystasia | A rare autosomal dominant neurological disorder with many of the clinical features of hereditary hypertrophic sensorimotor polyneuropathy combined with an essential tremor. Synonym: hereditary areflexic dystasia. (05 Mar 2000) |
| hereditary ataxia | A simple autosomal recessive trait in fox terrier dogs that produces a progressive general ataxia. (05 Mar 2000) |
| hereditary benign intraepithelial dyskeratosis | An autosomal dominant condition consisting of white spongy lesions of the buccal mucosa, floor of the mouth, ventral lateral tongue, gingiva and palate. Transient gelatinous plaques form over the cornea, which may produce temporary blindness, hereditary benign intraepithelial dyskeratosis. Synonym: hereditary benign intraepithelial dyskeratosis. (05 Mar 2000) |
| hereditary cerebellar ataxia | A disease of later childhood and early adult life, marked by ataxic gait, hesitating and explosive speech, nystagmus, and sometimes optic neuritis. It probably comprises several distinct conditions with diverse patterns of inheritance. Collective term for a number of hereditary disorders in which cerebellar signs are the most prominent finding. (05 Mar 2000) |
| hereditary chorea | A progressive disorder usually beginning in young to middle age, consisting of a triad of choreoathetosis, dementia, and autosomal dominant inheritance with complete penetrance. Bilateral marked wasting of the putamen and the head of the caudate nucleus is characteristic. Synonym: chronic progressive chorea, degenerative chorea, hereditary chorea, Huntington's disease. (05 Mar 2000) |
| hereditary coproporphyria | <haematology> A group of metabolic disorders that result from a disturbance in porphyrin metabolism, causing increased formation and excretion of porphyrin or its precursors. Acute intermittent porphyria is a rare inherited form that can result in abdominal pain, photosensitivity and neurological disturbances. The various forms can be differentiated measuring various blood prophyrins. Inheritance: autosomal dominant. (27 Sep 1997) |
| hereditary deafness and nephropathy | <nephrology, pathology> An inherited disorder involving damage to the kidneys, haematuria and hearing loss. In some individuals vision may also be affected. This genetic disease is uncommon. Symptoms include loss of hearing, abnormal colour to urine, swelling, cough and decline in vision. Inheritance: sex-linked autosomal dominant. Incidence: 1 in 50,000. Origin: Gr. Pathos = disease (27 Sep 1997) |
| hereditary deforming chondrodystrophy | A disturbance of enchondral bone growth in which multiple, generally benign osteochondromas of long bones appear during childhood, commonly with shortening of the radius and fibula; the ill-effects are usually mechanical but malignant change is rare; autosomal dominant inheritance. Synonym: diaphysial aclasis, hereditary deforming chondrodystrophy, multiple exostosis, osteochondromatosis. (05 Mar 2000) |
| hereditary exostosis | <radiology> (osteochondromatosis) Autosomal dominant, M more than F, multiple exostoses, snowflake calcification of mature cartilage cap, may leading to chondrosarcoma, short metacarpals (especially 4th and 5th) (12 Dec 1998) |
| hereditary fructose intolerance | A metabolic error due to deficiency of hepatic fructose 1,6-bisphosphate aldolase B (which also acts on fructose 1-phosphate); the second enzyme in the specific fructose pathway; vomiting and hypoglycaemia follow ingestion of fructose; prolonged fructose ingestion in young children results in failure to thrive and in jaundice, hepatomegaly, albuminuria, aminoaciduria, and sometimes cachexia and death; autosomal recessive inheritance in most families. (05 Mar 2000) |
| hereditary haemorrhagic telangiectasia | <gastroenterology> An inherited disease characterised by thin blood vessel walls in the nose, skin and gastrointestinal tract. This condition ins associated with a high risk of bleeding complications. Inheritance: autosomal dominant. (27 Sep 1997) |
| hereditary haemorrhagic thrombasthenia | <haematology> A form of congenital platelet functional defect that result in prolongation of the bleeding time. Characteristics include mucosal and post-operative bleeding that may be severe. (17 Dec 1997) |