| 영문 | cranial nerve | 한글 | 뇌신경 |
|---|---|---|---|
| 설명 | 대부분의 신경은 척수를 통해서 나간다. 그러나 몇몇의 신경은 뇌에서 바로 나간다. 이렇게 뇌에서 바로 나가는 신경을 뇌신경이라고 한다. 이 뇌신경은 12개로 모두 대칭적인 쌍으로 존재한다. 이 뇌신경은 주로 특수감각(시각, 청각, 후각, 미각)과 얼굴 등의 일부 근육을 지배하고 심장이나 내장의 지배도 일부 담당하고 있다. 12개의 신경은 각각 다음과 같은 이름과 고유번호를 가지고 있다. -후각신경(olfactory nerve)－후각을 담당하는 신경, -시각신경(optic nerve)－시각을 담당하는 신경. -눈돌림신경(oculomotor nerve)－운동을 담당하는 신경, -도르래신경(trochlear nerve)－눈의 운동을 담당하는 신경. -삼차신경(trigeminal nerve)－3개의 가지를 가지는 신경으로 얼굴의 감각과 씹기를 위한 근육을 움직이는 역할을 한다. -가돌림신경(abducent nerve)－눈의 운동을 담당하는 신경. -얼굴신경(facial nerve)－얼굴 근육의 운동을 담당하는 신경. 즉 얼굴이 여러 가지 표정을 내는 것은 이 신경의 작용이다. 그리고 혀의 앞부분의 미각을 담당하는 역할도 한다. -안뜰달팽이신경(vestibulocochlear nerve)－안뜰신경과 달팽이신경의 2가지 신경으로 이루어진 신경으로 모두 귀를 지배하는 신경이다. 안뜰신경은 평형감각을 담당하는 곳인 귀의 안뜰에서 나오는 신경으로 평형감각의 정보를 뇌에 전하는 역할을 한다. 그리고 달팽이신경은 청각을 감지하는 달팽이껍질의 모양을 가진 달팽이에서 기원하는 신경으로 청각의 정보를 뇌에 전달하는 역할을 한다. -혀인두신경(glossopharyngeal nerve)－말 그대로 혀와 인두부에 분포하는 신경으로 인후부의 움직임과 혀의 뒷부분의 미각을 담당한다. -미주신경(vagus nerve)－말 그대로 아주 여러 곳에 분포하여 분포영역이 모호한 신경이다(vagus란 모호한 이란 뜻을 가진다). 대부분의 내장에 분포하고 또 심장에 분포하여 심장의 박동수를 조정하는 역할도 한다. -더부신경(accessory nerve)－등의 근육과 목의 근육의 일부를 지배하는 신경. -혀밑신경(hypoglossal nerve)－혀의 움직임을 관장하는 신경. |
||
| 영문 | cranial cavity | 한글 | 두개강 |
|---|---|---|---|
| 설명 | 머리뼈 속의 공간으로 뇌가 들어가는 공간이다. |
||
| EC-IC bypass | Extra-Cranial Intra-Cranial bypass |
|---|---|
| CCT | carotid compression tomography; central conduction time; cerebrocranial trauma; chocolate-coated tab... |
| DMD | disease-modifying drug; Doctor of Dental Medicine; Duchenne muscular dystrophy; dystonia musculorum ... |
| DRD | dihydroxyphenylalanine-responsive dystonia; dorsal root dilator |
| ITD | idiopathic torsion dystonia; intensely transfused dialysis; iodothyronine deiodinase |
| CD | Cervical dystonia |
|---|---|
| DRD | DOPA responsive dystonia |
| ITD | Idiopathic torsion dystonia |
| OMD | Oromandibular dystonia |
| NCD | neurocirculatory dystonia |
| dystonia, cranial | A term used to describe dystonia that affects the muscles of the head, face, and neck. Oromandibular dystonia affects the muscles of the jaw, lips, and tongue. The jaw may be pulled either open or shut, and speech and swallowing can be difficult. Spasmodic dysphonia involves the muscles of the throat that control speech. Also called spastic dysphonia or laryngeal dystonia, it causes strained and difficult speaking or breathy and effortful speech. Meige's syndrome is the combination of blepharospasm and oromandibular dystonia and sometimes spasmodic dysphonia. Spasmodic torticollis can be classified as a type of cranial dystonia. (12 Dec 1998) |
|---|
| cranial dystonia | <neurology> A term used to describe dystonia that affects the muscles of the head, face, and neck. Oromandibular dystonia affects the muscles of the jaw, lips, and tongue. The jaw may be pulled either open or shut, and speech and swallowing can be difficult. Spasmodic dysphonia involves the muscles of the throat that control speech. Also called spastic dysphonia or laryngeal dystonia, it causes strained and difficult speaking or breathy and effortful speech. Meige's syndrome is the combination of blepharospasm and oromandibular dystonia and sometimes spasmodic dysphonia. Spasmodic torticollis can be classified as a type of cranial dystonia. (12 Dec 1998) |
|---|---|
| segawa's dystonia | An important variant of dopa-responsive dystonia (drd). Typically, drd begins in childhood or adolescence with progressive difficulty in walking and, in some cases, spasticity. In segawa's dystonia, the symptoms fluctuate during the day from relative mobility in the morning to increasingly worse disability in the afternoon and evening as well as after exercise. (12 Dec 1998) |
| dementia-nuchal dystonia | 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) |
| dopa-responsive dystonia | A condition successfully treated with drugs. Typically, DRD begins in childhood or adolescence with progressive difficulty in walking and, in some cases, spasticity. Segawa's dystonia is an important variant of DRD. In Segawa's dystonia, the symptoms fluctuate during the day from relative mobility in the morning to increasingly worse disability in the afternoon and evening as well as after exercise. Some scientists feel DRD is not only rare but also rarely diagnosed since it mimics many of the symptoms of cerebral palsy. (12 Dec 1998) |
| dystonia | <clinical sign, neurology> Disordered tonicity of muscle. Origin: Gr. Tonos (18 Nov 1997) |
| dystonia, dopa-responsive | A condition successfully treated with drugs. Typically, DRD begins in childhood or adolescence with progressive difficulty in walking and, in some cases, spasticity. Segawa's dystonia is an important variant of DRD. In Segawa's dystonia, the symptoms fluctuate during the day from relative mobility in the morning to increasingly worse disability in the afternoon and evening as well as after exercise. Some scientists feel DRD is not only rare but also rarely diagnosed since it mimics many of the symptoms of cerebral palsy. (12 Dec 1998) |
| dystonia, focal, due to blepharospasm | The second most common focal dystonia, the involuntary, forcible closure of the eyelids. The first symptoms may be uncontrollable blinking. Only one eye may be affected initially, but eventually both eyes are usually involved. The spasms may leave the eyelids completely closed causing functional blindness even though the eyes and vision are normal. (12 Dec 1998) |
| dystonia, focal, due to torticollis | Spasmodic torticollis, or torticollis, is the most common of the focal dystonias. In torticollis, the muscles in the neck that control the position of the head are affected, causing the head to twist and turn to one side. In addition, the head may be pulled forward or backward. (12 Dec 1998) |
| dystonia, idiopathic torsion | A form of dystonia known as early-onset torsion dystonia (also called generalised torsion dystonia) begins in childhood around the age of 12. Symptoms typically start in one part of the body, usually in an arm or leg, and eventually spread to the rest of the body within about 5 years. Early-onset torsion dystonia is not fatal, but it can be severely debilitating. (12 Dec 1998) |
| dystonia lenticularis | Dystonia resulting from a lesion of the lenticulate nucleus. (05 Mar 2000) |
| dystonia musculorum deformans | A genetic, environmental, or idiopathic disorder, usually beginning in childhood or adolescence, marked by muscular contractions that distort the spine, limbs, hips, and sometimes the cranial-innervated muscles. The abnormal movements are increased by excitement and, at least initially, abolished by sleep. The musculature is hypertonic when in action, hypotonic when at rest. Hereditary forms usually begin with involuntary posturing of the foot or hand (autosomal recessive form ) or of the neck or trunk (autosomal dominant form ); both forms may progress to produce contortions of the entire body. Synonym: progressive torsion spasm, torsion disease of childhood, torsion dystonia, Ziehen-Oppenheim disease. (05 Mar 2000) |
| dystonia, oromandibular | Oromandibular dystonia affects the muscles of the jaw, lips, and tongue. The jaw may be pulled either open or shut, and speech and swallowing can be difficult. (12 Dec 1998) |
| dystonia, segawa's | An important variant of dopa-responsive dystonia (DRD), a condition successfully treated with drugs. Typically, DRD begins in childhood or adolescence with progressive difficulty in walking and, in some cases, spasticity. In Segawa's dystonia, the symptoms fluctuate during the day from relative mobility in the morning to increasingly worse disability in the afternoon and evening as well as after exercise. (12 Dec 1998) |
| dystonia, torsion | A form of dystonia known as early-onset torsion dystonia (also called idiopathic or generalised torsion dystonia) begins in childhood around the age of 12. Symptoms typically start in one part of the body, usually in an arm or leg, and eventually spread to the rest of the body within about 5 years. Early-onset torsion dystonia is not fatal, but it can be severely debilitating. most children with the disorder are unable to perform the simplest of motor tasks and are confined to a wheelchair by the time they reach adulthood. (12 Dec 1998) |
| dystonia, writer's cramp | 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) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|