| 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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| 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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| INCD | infantile nuclear cerebral degeneration |
|---|---|
| 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; ... |
| CT | calcitonin; calf testis; cardiac tamponade; cardiothoracic [ratio]; carotid tracing; carpal tunnel; ... |
| progressive bulbar palsy | One of the subgroups of motor neuron disease; a progressive degenerative disorder of the motor neurons of primarily the brainstem, manifested as weakness (and wasting) of the various bulbar muscles, resulting in dysarthria and dysphagia-fluid regurgitation is an outstanding symptom and can cause aspiration; tongue weakness and wasting is usually evident, and often the fasciculation potentials are present in the tongue and facial muscles. Synonym: glossopalatolabial paralysis, glossopharyngeolabial paralysis. (05 Mar 2000) |
|---|---|
| progressive supranuclear palsy | A disorder that is associated with nerve cell destruction and progressive lack of coordination, neck stiffness, trunk stiffness, problems with eye movement and mild dementia. Disorders that are similar include Alzheimer's disease, cerebellar dysfunction, Jakob-Creutzfeldt disease and Parkinson's disease. The cause for progressive supranuclear palsy is unknown, but is likely a degenerative nerve disorder that is somehow triggered by a viral infection. Pathologic changes include nerve cell damage and destruction of myelin sheath. There is no known cure. (27 Sep 1997) |
| scrivener's palsy | A dystonia that affects the muscles of the hand and sometimes the forearm and only occurs during handwriting. Similar focal dystonias have also been called typist's cramp, pianist's cramp, musician's cramp, and golfer's cramp. (12 Dec 1998) |
| supranuclear palsy, progressive | A progressive neurological disease usually of the fifth decade characterised by supranuclear ophthalmoplegia especially paralysis of downward gaze, pseudobulbar palsy, gait disturbance, dysathria, truncal dystonia, memory and personality deterioration, and dementia. (12 Dec 1998) |
| Dejerine-Klumpke palsy | A type of brachial birth palsy in which there is paralysis of the muscles of the distal forearm and hand (all ulnar innervated muscles, plus more distal radial and median-innervated muscles), due to a lesion of the lower trunk of the brachial plexus, or of the C8 and T1 cervical roots. Synonym: Dejerine-Klumpke palsy, Dejerine-Klumpke syndrome, Klumpke's paralysis. (05 Mar 2000) |
| diver's palsy | A disorder characterised by joint pains, respiratory manifestations, skin lesions, and neurologic signs, occurring in aviators flying at high altitudes and following rapid reduction of air pressure in persons who have been breathing compressed air in caissons and diving apparatus. (12 Dec 1998) |
| obstetrical palsy | A brachial plexus lesion sustained by the infant during the birthing process; three types are recognised: 1) upper plexus type, affects the shoulder and upper arm (Erb palsy); 2) total plexus type, involves the whole arm; 3) lower plexus type, involves the forearm and hand (Klumpke palsy). Synonym: obstetrical paralysis. (05 Mar 2000) |
| trembling palsy | <neurology> A group of neurological disorders characterised by hypokinesia, tremor and muscular rigidity. (18 Nov 1997) |
| Erb palsy | A type of brachial birth palsy in which there is paralysis of the muscles of the upper arm and shoulder girdle (deltoid, biceps, brachialis, and brachioradialis muscles) due to a lesion of the upper trunk of the brachial plexus or of the roots of the fifth and sixth cervical roots. Synonym: Duchenne-Erb paralysis, Erb paralysis. (05 Mar 2000) |
| facial palsy | <neurology> A condition that involves the facial nerve (VII cranial nerve) and results in the paralysis of one side of the face. Bell's (facial nerve palsy) can be differentiated from a central (stroke) deficit by the inability to raise the eyebrow on the affected side. (27 Sep 1997) |
| Klumpke palsy | A type of brachial birth palsy in which there is paralysis of the muscles of the distal forearm and hand (all ulnar innervated muscles, plus more distal radial and median-innervated muscles), due to a lesion of the lower trunk of the brachial plexus, or of the C8 and T1 cervical roots. Synonym: Dejerine-Klumpke palsy, Dejerine-Klumpke syndrome, Klumpke's paralysis. (05 Mar 2000) |
| lead palsy | Paralysis of the extensor muscles of the wrist causing wrist-drop; occurs in lead poisoning. Synonym: lead paralysis. (05 Mar 2000) |
| aggressive infantile fibromatosis | A childhood counterpart of abdominal or extra-abdominal desmoid tumours, characterised by firm subcutaneous nodules that grow rapidly in any part of the body that invade locally and recur but do not metastasize. (05 Mar 2000) |
| autism, infantile | A syndrome beginning in infancy and characterised by a lack of responsiveness to other people, gross impairment in verbal and nonverbal communication skills, and bizarre responses to the environment. (12 Dec 1998) |
| progressive infantile spinal muscular atrophy | Transmitted as autosomal recessive on chromosome 5q. Progressive dysfunction of the anterior horn cells in the spinal cord and brainstem cranial nerves with profound weakness and bulbar dysfunction occurring in the first two years of life. Three groups, based on age of clinical onset, are recognised. Synonym: familial spinal muscular atrophy, Hoffmann's muscular atrophy, infantile muscular atrophy, infantile progressive spinal muscular atrophy, progressive infantile spinal muscular atrophy, Werdnig-Hoffmann disease, Werdnig-Hoffmann muscular atrophy. (05 Mar 2000) |