| 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. |
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| 영문 | cranial cavity | 한글 | 두개강 |
|---|---|---|---|
| 설명 | 머리뼈 속의 공간으로 뇌가 들어가는 공간이다. |
||
| ECG | Electro-Cardio-Graphy(-Gram); 심전도 = EKG 1. Conducting System Structu... |
|---|---|
| VIIag | factor VII antigen |
| EC-IC bypass | Extra-Cranial Intra-Cranial bypass |
| CCT | carotid compression tomography; central conduction time; cerebrocranial trauma; chocolate-coated tab... |
| CN | Cranial Nerve |
| Endo VII | Endonuclease VII |
|---|---|
| F VII:Ag | F VII antigen |
| F VII | Factor VII |
| F VII:C | Factor VII activity |
| MPS VII | Mucopolysaccharidosis Type VII |
| cranial mononeuropathy vii | A disorder which involves drooping of the face and the decreased ability to move one side of the face. Causes include isolated damage to the facial nerve, HIV infection, sarcoidosis and Lyme disease. Bell's palsy is a dysfunction of the facial nerve for reason unknown. (27 Sep 1997) |
|---|
| cranial mononeuropathy III | (compression type) A disorder involving vision changes and eyelid drooping associated with a decreased functioning of cranial nerve III. Damage is usually caused by compression of the nerves from localised lesions or a swelling in the area of the nerve. Examples include cerebral aneurysms and tumours Symptoms include a drooping eyelid and double vision. (diabetic type) A disorder involving vision changes and eyelid drooping associated with a decreased functioning of cranial nerve III as a complication of diabetes. Symptoms include a drooping eyelid and double vision. Good control of blood sugars can reduce the incidence of this complication. (27 Sep 1997) |
|---|---|
| cranial mononeuropathy vi | A disorder involving vision changes that are associated with the decreased function of cranial nerve VI. Often this form of nerve damage is associated with diabetes, tumours of the VI nerve or increased intracranial pressure. Trauma and stroke may also damage the VI cranial nerve. Symptoms include double vision when looking to one side. (27 Sep 1997) |
| cranial nerve VII | <anatomy, nerve> The facial nerve enervates the muscles of the face (facial expression). Lesion of the facial nerve cause a drooping to one side of the face, inability to wrinkle the forehead, inability to whistle, inability to close the eye and deviation of the mouth to the unaffected side. Synonym: cranial nerve VII. (27 Sep 1997) |
| mononeuropathy | Disorder involving a single nerve. Mononeuropathy multiplex, inflammation of several nerves usually in unrelated portions of the body. (05 Mar 2000) |
| annexin vii | Protein of the annexin family that promotes the aggregation and fusion of chromaffin granules and can also act as a voltage-dependent calcium channel. (12 Dec 1998) |
| glycogen storage disease type VII | <disease> An autosomal recessive muscle glycogen storage disease in which there is deficient expression of muscle phosphofructokinase activity, resulting in increased concentrations of glucose-6-phosphate and fructose-6-phosphate and low concentrations of fructose-1,6-diphosphate in muscle tissue. Glycogen storage in muscle is increased, perhaps due to activation of glycogen synthase by accumulated glucose-6-phosphate. It has been proposed that shunting of glucose-6-phosphate and fructose-6-phosphate into the pentose phosphate pathway may result in increased synthesis of purines and pyrimidines, causing hyperuricaemia and gout. Erythrocytes from patients may show decreased phosphofructokinase activity and 2,3-diphosphoglycerate deficiency. Exercise intolerance is present and severe congenital muscular dystrophy has been reported. Inheritance: autosomal recessive (12 Dec 1998) |
| mucopolysaccharidosis vii | Mucopolysaccharidosis characterised by excessive dermatan and heparan sulfates in the urine and hurler-like features. It is caused by a deficiency of beta-glucuronidase. (12 Dec 1998) |
| type VII mucopolysaccharidosis | <syndrome> An autosomal recessive disorder due to a deficiency of a beta-glucuronidase; defective lysosomal degradation of dermatan sulfate, heparan sulfate, and chondroitin sulfate; cellular function disrupted in most tissues. Synonym: type VII mucopolysaccharidosis, type VIII mucopolysaccharidosis. (05 Mar 2000) |
| exonuclease vii | An exonuclease enzyme which makes oligonucleotides by cleaving chunks of nucleotides off of both ends of single-stranded DNA. (09 Oct 1997) |
| factor vii | <chemical> Heat- and storage-stable plasma protein that is activated by tissue thromboplastin to form factor viia in the extrinsic pathway of blood coagulation. The activated form then catalyses the activation of factor x to factor xa. Chemical name: Blood-coagulation factor VII (12 Dec 1998) |
| factor vii assay | A test used to measure the activity of a blood clotting factor VII. This test may be used to evaluate excessive bleeding. Abnormally low factor VII assays may be seen in the following conditions: congenital deficiency of factor VII, fat malabsorption, heparin administration, cirrhosis, vitamin K deficiency and warfarin administration. (27 Sep 1997) |
| factor vii deficiency | An inherited disorder that causes abnormal blood clotting due to the congenital absence of one of the 20 different plasma proteins involved in the coagulation process. Symptoms include bleeding of the gums, nosebleeds, easy bruising, bleeding in muscles or joints and excessive menstrual bleeding. Treatment includes the administration of plasma concentrates of factor VII (extrinsic factor). (27 Sep 1997) |
| anterior cranial base | The portion of the internal base of the skull, anterior to the sphenoidal ridges and limbus, in which the frontal lobes of the brain rest. Synonym: fossa cranii anterior, anterior cranial base. (05 Mar 2000) |
| anterior cranial fossa | The portion of the internal base of the skull, anterior to the sphenoidal ridges and limbus, in which the frontal lobes of the brain rest. Synonym: fossa cranii anterior, anterior cranial base. (05 Mar 2000) |
| attached cranial section | Craniotomy with a segment of the calvaria and attached soft tissues turned as a flap to expose the cranial cavity. Synonym: attached cranial section, osteoplastic craniotomy. (05 Mar 2000) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|