| 영문 | chorea | 한글 | 무도병 |
|---|---|---|---|
| 설명 | 주로 사지의 세밀한 불규칙한 불수의 운동이 다양하게 반복되는 것으로 얼굴을 찡그리거나 혀의 움직임을 동반한다. 얼굴-손-발-혀 따위가 뜻대로 되지 않고 저절로 심하게 움직여, 마치 춤을 추는 듯한 모습이 되는 신경병. 소무도병-헌팅턴무도병-노인성 무도병 따위가 있는데, 걸리는 연령층과 원인이 다르다. 류마티스열이 있을 때나 바닥핵의 병터가 있을 때 나타난다. 동작이 의도적으로 보이나, 실제로는 어떤 충동이나 외부자극에 반응하여 의지와는 전연 무관하게 행해지는 것을 특징으로 한다. 류마티스에 관련하여 일어나는 피라밋외로계 병의 하나로, 그 보행이 마치 춤을 추는 것 같아서 붙은 이름이다. 여성, 특히 소녀에게 많은 시데남무도병(소무도병)은 고치기 쉬우나 중년에 시작되는 유전성인 것은 정신장애가 따르고 진행성이어서 치유가 어렵다. 무릎관절의 앞쪽에 따로 떨어져 존재하는 조그만 뼈, 흔히 밖에서도 손으로 촉지된다. |
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| CHO | carbohydrate; Chinese hamster ovary; chorea |
|---|---|
| FACWA | familial amyotrophic chorea with acanthocytosis |
| HC | hair cell; hairy cell; handicapped; head circumference; head compression; health care; healthy contr... |
| HSP | Henoch Schonlein Purpura |
| HS | Haber syndrome; half strength; hamstring; hand surgery; Hartmann solution; head sling; healthy subje... |
| HC | Huntington chorea |
|---|---|
| SC | Sydenham chorea |
| HSP | Henoch Schonlein Purpura |
| HSPN | Henoch-Schoenlein purpura nephritis |
| SHP | Scholein-Henoch purpura |
| Henoch's chorea | A disorder in which sudden spasmodic coordinated movements of certain muscles or groups of physiologically related muscles occur at irregular intervals. Synonym: Henoch's chorea. (05 Mar 2000) |
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| Henoch, Eduard | <person> German paediatrician, 1820-1910. See: Henoch's chorea, Henoch's purpura, Henoch-Schonlein purpura, Henoch-Schonlein syndrome, Schonlein-Henoch syndrome. (05 Mar 2000) |
|---|---|
| henoch-schoenlein syndrome | <radiology> Acute, self-limited arteritis, often follows Strep infection, symptoms: purpura, nephritis, abdominal pain, joint pain, thick small bowel folds, thumbprinting in small bowel or colon (12 Dec 1998) |
| Henoch-Schonlein purpura | <dermatology> This relatively rare disorder is characterised by skin purpura, joint pains, abdominal pain and renal disease (glomerulonephritis). Although Henoch-Schonlein purpura or anaphylactoid purpura, is thought to be a immune complex mediated disease, its exact cause is unknown. Its typical benign coarse can, however, include renal failure. (27 Sep 1997) |
| Henoch-Schonlein syndrome | <dermatology> This relatively rare disorder is characterised by skin purpura, joint pains, abdominal pain and renal disease (glomerulonephritis). Although Henoch-Schonlein purpura or anaphylactoid purpura, is thought to be a immune complex mediated disease, its exact cause is unknown. Its typical benign coarse can, however, include renal failure. (27 Sep 1997) |
| Henoch's purpura | <dermatology> This relatively rare disorder is characterised by skin purpura, joint pains, abdominal pain and renal disease (glomerulonephritis). Although Henoch-Schonlein purpura or anaphylactoid purpura, is thought to be a immune complex mediated disease, its exact cause is unknown. Its typical benign coarse can, however, include renal failure. (27 Sep 1997) |
| Schonlein-Henoch syndrome | <dermatology> This relatively rare disorder is characterised by skin purpura, joint pains, abdominal pain and renal disease (glomerulonephritis). Although Henoch-Schonlein purpura or anaphylactoid purpura, is thought to be a immune complex mediated disease, its exact cause is unknown. Its typical benign coarse can, however, include renal failure. (27 Sep 1997) |
| purpura, henoch-schonlein | HSP is a form of blood vessel inflammation, a vasculitis that affects small arterial vessels in the skin (capillaries) and the kidneys. Hsp results in skin rash associated with joint inflammation (arthritis) and cramping pain in the abdomen. Hsp frequently follows a bacterial or viral infection of the throat or breathing passages and is an unusual reaction of the body's immune system to this infection. Hsp occurs most commonly in children. Hsp is generally a mild illness that resolves spontaneously, but sometimes it can cause serious problems in the kidneys and bowels. Treatment is directed toward the most significant area of involvement. Joint pain can be relieved by antiinflammatory medications, such as aspirin or ibuprofen. Some patients can require cortisone-related medications, such as prednisone, especially those with significant abdominal pain or kidney disease. Also known as anaphylactoid purpura. (12 Dec 1998) |
| purpura, schoenlein-henoch | A form of nonthrombocytopenic purpura due to a hypersensitivity vasculitis (vasculitis, hypersensitivity) associated with a variety of clinical symptoms including urticaria and erythema, arthropathy and arthritis, gastrointestinal symptoms, and renal involvement. (12 Dec 1998) |
| acanthocytosis with chorea | A slowly progressive familial chorea with associated mental deterioration, diminished deep tendon reflexes, bilateral atrophy of the putamen and caudate nuclei and acanthocytosis (thorny appearance of blood erythrocytes); the disorder typically begins around late adolescence; inheritance is usually autosomal recessive. Synonym: acanthocytosis with chorea. (05 Mar 2000) |
| acute chorea | A postinfectious chorea appearing several months after a streptococcal infection with subsequent rheumatic fever. The chorea typically involves the distal limbs and is associated with hypotonia and emotional lability. Improvement occurs over weeks or months and exacerbations occur without associated infection recurrence. Synonym: acute chorea, chorea minor, chorea, juvenile chorea, rheumatic chorea, Sydenham's disease. (05 Mar 2000) |
| benign familial chorea | A rare, nonprogressive movement disorder characterised by chorea and athetosis appearing in early childhood, most commonly manifested as gait ataxia and upper limb coordination. Intellect is unaffected. Probably autosomal-dominance inheritance with incomplete penetrance. (05 Mar 2000) |
| rheumatic chorea | A postinfectious chorea appearing several months after a streptococcal infection with subsequent rheumatic fever. The chorea typically involves the distal limbs and is associated with hypotonia and emotional lability. Improvement occurs over weeks or months and exacerbations occur without associated infection recurrence. Synonym: acute chorea, chorea minor, chorea, juvenile chorea, rheumatic chorea, Sydenham's disease. (05 Mar 2000) |
| rhythmic chorea | Patterned movement in conversion hysteria. (05 Mar 2000) |
| chorea | Mature onset disease characterised by progressive loss of neuronal functioning. Caused by unstable amphlification of a trinucleotide (CAG)n repeat with the coding region of a gene encoding a 348 kD, widely exposed product. (18 Nov 1997) |
| chorea-acanthocytosis | A slowly progressive familial chorea with associated mental deterioration, diminished deep tendon reflexes, bilateral atrophy of the putamen and caudate nuclei and acanthocytosis (thorny appearance of blood erythrocytes); the disorder typically begins around late adolescence; inheritance is usually autosomal recessive. Synonym: acanthocytosis with chorea. (05 Mar 2000) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|