| 영문 | muscular system | 한글 | 근육계통 |
|---|---|---|---|
| 설명 | 근육에 의해 이루어진 하나의 계통을 임의적으로 나누어 부른 말. |
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| 영문 | muscular dystrophy | 한글 | 근육퇴행위축 |
|---|---|---|---|
| 설명 | 근섬유의 파괴로 인한 점진적인 근위축과 허약을 특징으로 하는 일련의 선천적인 질환군을 통털어 말한다. 대표적인 경우가 뒤쉔(Duchenne)형으로 성염색체 열성유전을 하며, 대개 4 세이내에 발병해 청년기를 넘기는 경우가 드물다. 특징적 소견으로 장딴지근(gastronemius)의 거짓비대(pseudohypertrophy)(실제적으로는 근위축이 일어나지만, 근섬유 대신에 지방세포가 들어차 도리어 마치 근육이 증가한 것처럼 보이는 현상) 소견을 볼 수 있다. |
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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 | artery | 한글 | 동맥 |
|---|---|---|---|
| 설명 | 심장에서 나오는 피를 운반하는 혈관을 말한다. |
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| 영문 | carotid artery | 한글 | 목동맥 |
|---|---|---|---|
| 설명 | 머리부분의 혈액을 공급하는 동맥. 온목동맥는 대동맥에서 직접 나오는 동맥으로, 바깥목동맥와 속목동맥로 나뉜다. 속목동맥은 뇌의 혈액을 공급하는 역할을 하고, 바깥목동맥은 뇌를 제외한 머리부분에 혈액을 공급하는 역할을 한다. |
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| ECG | Electro-Cardio-Graphy(-Gram); 심전도 = EKG 1. Conducting System Structu... |
|---|---|
| PMD | Progressive Muscular Dystrophy; 진행성 근이영양증 Types of PMD(Progressive Muscular Dystroph... |
| TAPVR | Total Anomalous Pulmonary Venous Return = TAPVC 4 Types of TAPVR &... |
| VSD | Ventricular Septal Defect ? Types of VSD 1. Subpulmonic(=... |
| ALL | Acute Lymphocytic Leukemia 형태학적 분류 L1; Small, Homogenous(... |
| DMD | Duchenne type muscular dystrophy |
|---|---|
| FCMD | Fukuyama type congenital muscular dystrophy |
| ALCA-PA | Anomalous origin of the left coronary artery from the pulmonary artery |
| STA-MCA | Superficial temporal artery - middle cerebral artery |
| STA-MCA | Superficial temporal artery to middle cerebral artery |
| Becker type muscular dystrophy | A muscular dystrophy that has many of the clinical features of Duchenne muscular dystrophy e.g., symmetrical involvement of first the pelvicrural muscles and then the pectoral girdle and proximal upper extremity muscles; pseudohypertrophy, especially of the calf muscles but with a much later age of onset (35-45 years), and more benign course. X-linked inheritance. (05 Mar 2000) |
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| Becker type tardive muscular dystrophy | Muscular dystrophy of late onset, often in the second or third decade, with relatively mild course; X-linked recessive inheritance; perhaps allelic with Duchenne's dystrophy, but milder and not a genetic lethal. Compare: Duchenne dystrophy. Synonym: Becker type tardive muscular dystrophy. (05 Mar 2000) |
| muscular artery | <anatomy, artery> An artery with a tunica media composed principally of circularly arranged smooth muscle. Synonym: distributing artery, medium artery. (05 Mar 2000) |
| anastomotic branch of middle meningeal artery to lacrimal artery | <anatomy, artery> A branch of the middle meningeal artery arising in the cranial cavity which runs anteriorly through the superior orbital fissure to anastomose with the lacrimal artery. See: orbital branch of middle meningeal artery. Synonym: ramus anastomoticus arteriae meningeae mediae cum lacrimali. (05 Mar 2000) |
| adult pseudohypertrophic muscular dystrophy | Muscular dystrophy of late onset, often in the second or third decade, with relatively mild course; X-linked recessive inheritance; perhaps allelic with Duchenne's dystrophy, but milder and not a genetic lethal. Compare: Duchenne dystrophy. Synonym: Becker type tardive muscular dystrophy. (05 Mar 2000) |
| Becker's muscular dystrophy | An X-linked inherited disorder characterised by slowly progressive muscle weakness of the legs and pelvis. Other symptoms and findings include increased difficulty walking, intellectual retardation, fatigue and pseudohypertrophy of the calf muscles. (27 Sep 1997) |
| benign pseudohypertrophic muscular dystrophy | <neurology> An X-linked inherited disorder characterised by slowly progressive muscle weakness of the legs and pelvis. Other symptoms and findings include increased difficulty walking, intellectual retardation, fatigue and pseudohypertrophy of the calf muscles. (06 Aug 1998) |
| pelvofemoral muscular dystrophy | One of the less well-defined types of muscular dystrophy, probably heterogenous in nature. Onset usually in childhood or early adulthood and both sexes affected. Characterised by weakness and wasting, usually symmetrical, of the pelvic girdle muscles, the shoulder girdle muscles, or both, but not the facial muscles. Muscle pseudohypertrophy, heart involvement, and mental retardation are absent. Variable inheritance. Synonym: Leyden-Mobius muscular dystrophy, pelvofemoral muscular dystrophy, scapulohumeral muscular dystrophy. (05 Mar 2000) |
| childhood muscular dystrophy | The most common childhood muscular dystrophy, with onset usually before age 6. Characterised by symmetrical weakness and wasting of first the pelvic and crural muscles and then the pectoral and proximal upper extremity muscles; pseudohypertrophy of some muscles, especially the calf; heart involvement; sometimes mild mental retardation; progressive course and early death, usually in adolescence. X-linked inheritance (affects males and transmitted by females). Synonym: childhood muscular dystrophy, Duchenne's disease, pseudohypertrophic muscular dystrophy. (05 Mar 2000) |
| peroneal muscular atrophy | A group of three familial peripheral neuromuscular disorders, sharing the common feature of marked wasting of the more distal extremities, particularly the peroneal muscle groups, resulting in "stork legs." Two of the three subtypes are hereditary sensorimotor polyneuropathies, one demyelinating in type and the other axon loss in type, while the third subgroup is an anterior horn cell disorder. It usually involves the legs before the arms; pes cavus is often the first sign; autosomal dominant, autosomal recessive, and X-linked recessive types, with severity related to genetic type. Synonym: Charcot-Marie-Tooth disease. (05 Mar 2000) |
| circular layer of muscular coat | The inner, circular layer of the smooth muscle of the muscular coat. Nomina Anatomica lists circular layers of muscular coats (stratum circulare tunicae muscularis...) of the following: 1) colon (... Coli ); 2) rectum (... Recti ); 3) small intestine (... Intestini tenuis ); 4) stomach (... Gastrici ). Synonym: stratum circulare tunicae muscularis gastricae, stratum circulare tunicae. (05 Mar 2000) |
| circular layers of muscular tunics | The inner, circular layer of the smooth muscle of the muscular coat. Nomina Anatomica lists circular layers of muscular coats (stratum circulare tunicae muscularis...) of the following: 1) colon (... Coli ); 2) rectum (... Recti ); 3) small intestine (... Intestini tenuis ); 4) stomach (... Gastrici ). Synonym: stratum circulare tunicae muscularis gastricae, stratum circulare tunicae. (05 Mar 2000) |
| Werdnig-Hoffmann 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) |
| muscular | <anatomy> Pertaining to or composing muscle. Origin: L. Muscularis (18 Nov 1997) |
| muscular asthenopia | Asthenopia due to imbalance of the extrinsic ocular muscles. (05 Mar 2000) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|